Position

Are you a passionate Software Engineer looking to bring cutting-edge software solutions to drug discovery? Join our mission to bring novel therapeutics to patients and be at the forefront of driving innovation through technology. As a Software Engineer 2, you will leverage your expertise to develop and implement software solutions that drive our groundbreaking scientific initiatives.

About You

The ideal candidate for this role thrives at the intersection of software and scientific discovery. You are proficient with production-quality Python codebases and can contribute to, maintain, and extend these codebases in a robust and scalable way. At the same time, you understand the fast pace of scientific discovery, and can collaborate with scientists to clarify requirements, focus on result rather than implementation, and keep projects moving forward. You are a strong communicator, especially to non-engineers, as well as a strong team player, always ready to pitch in to help a colleague. You are a continual learner with a growth mindset, eager to learn from your colleagues and expand your talents in a supportive environment and are excited about our mission to bring drugs to patients.

What You’ll Do

• Work with scientists to understand data generated by early drug discovery projects and provide custom analyses and/or production software solutions to answer key questions about the data.
• Build, maintain, and extend tools that deliver machine-learning-based as well as classical algorithmic solutions to scientists.
• Contribute to the continuous improvement of software development processes, tools, and methodologies.
• Conduct thorough code reviews, promoting best practices and identifying opportunities for code optimization and enhancement.
• Collaborate with team members, sharing insights and fostering a culture of knowledge sharing and learning.
• Uphold ethical and data privacy standards in all software engineering activities.

Qualifications

• BS in Computer Science, Mathematics, Physics, Bioinformatics, Biophysics, or a related field, plus 2 years of relevant experience, or equivalent work experience.
• Demonstrated experience (2+ years) with Python; familiarity with scientific programming packages (pandas, numpy) and/or machine learning frameworks (TensorFlow) a plus.
• Undergraduate level biology knowledge required; experience manipulating and analyzing biologically relevant data sets strongly desired (e.g. sequencing data, cellular imaging data, etc).
• Introductory coursework on deep learning or other modern ML approaches, or equivalent work experience, a plus.
• Familiarity with basic software best practices (CI/CDD, unit testing, version control, etc.) highly preferred.
• Strong analytical and problem-solving skills, with the ability to think critically and creatively to overcome technical challenges.
• Effective communication skills to collaborate with diverse teams, both technical and non-technical, especially across disciplines.
• Demonstrated ability to thrive in a fast-paced, dynamic work environment.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $135,000 to $147,250 depending on skills, competency, and the market demand for your expertise.

Position 

The Software Engineering Manager, Data Engineering will join a multi-disciplinary engineering team that develops systems handling multiple high-throughput (PB/week) high-content imaging data streams. The position's primary responsibility will be to lead a small team to design and support mission-critical computational pipelines to analyze proprietary microscopy data, in collaboration with the larger Engineering, Research and Information Technology teams. 

About You 

You are a software engineer at heart who enjoys discussing architecture and data design with senior peers. You actively code and collaborate while keeping team goals aligned with business objectives. 

What You will Do 

• Manage a small team of software engineers.
• Maintain essential computational pipelines and applications for ongoing scientific research.
• Build reliable, flexible data processing and data storage architecture to organize biological and microscopy datasets and extract features from Eikon’s proprietary data.
• Work with data lakes and data pipelines to organize, clean, and serve scientific data for diverse use cases.
• Define and evolve the engineering system architecture vision to support system features and user-facing capabilities.
• Characterize and communicate design trade-offs to technical and non-technical audiences.
• Collaborate with Product and Program Management to develop high-level roadmaps for key software deliverables satisfying defined system-level business needs and user acceptance tests.
• Stay up to date with emerging trends and advancements in machine learning, distributed systems, cloud technologies, and software engineering practices, and evaluate their potential impact on our internal products.

Qualifications 

• Bachelor's degree with 15 years of relevant experience or a master's degree with 12 years of relevant experience or a PhD with 8 years of relevant experience in Computer Science, Software Engineering or a related field.
• Prior management and leadership experience.
• Prior experience building and supporting reliable production data pipelines.
• Strong proficiency in Postgres, Python, React, TypeScript. 
• Experience in multiple strongly typed languages such as C++, C# or Java.
• Successful track record designing software and systems architecture, including API and database design, commercial application development, cloud services, and DevOps practices.
• Experience with architecting and building analysis software.
• Excellent verbal and written communication skills, ability to bridge the gap between scientific users, engineers and developers. 
• Team-oriented, flexible, able to adapt to rapidly evolving goals and challenges. 
• Demonstrated leadership skills in a changing organization with evolving processes.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $183,000 to $199,500 depending on skills, competency, and the market demand for your expertise.

Position  

The Hardware group at Eikon Therapeutics develops super-resolution, high-throughput optical instrumentation. The Hardware team is seeking a Senior Electrical Engineer to participate in future instrument development. As part of Eikon’s diverse team of biologists, medicinal chemists, hardware, and software engineers, you will design and deploy custom super-resolution microscopes and automated systems that will enable the exploration and quantification of Eikon’s high-content datasets. 

About you

You are an adventurous, passionate, and creative electrical engineer eager to apply your talents to empower a new way of discovering medicines in a highly interdisciplinary biopharmaceutical environment. You are excited about the challenges of developing cutting-edge hardware from the ground up to enable novel technologies and solve real-world problems, and you will bring to these challenges enthusiasm, high energy, intellectual curiosity, and technical excellence.

What you’ll do

• Join an engineering team designing super-resolution microscopes, including signal processing, motion control, robotics and system automation that enables Eikon’s scientific achievements
• Contribute to system design architecture of instrument control and data acquisition systems
• Design, prototype, and test electronic assemblies. Work closely with the microscopy and automation teams on design validation, implementation, and design improvements 
• Write FPGA and microcontroller firmware to implement required functionality. Write PC host code to test and characterize your design
• Build and release assemblies to be used by scientists and end-users, creating a full suite of documentation and test procedures 

Qualifications

• Bachelor's degree with 5 years of relevant experience or a Master’s degree with 3 years of relevant experience designing complex digital and analog circuity
• Systems design experience contributing to design architecture
• Ability and desire to bring your design through all stages including directing PCBA layout, working with contract manufacturers, testing, debugging and rework of high density PCBAs with fine pitch components 
• Strong experience debugging systems using oscilloscopes and logic analyzers
• Hands-on experience building test set-ups, reworking and modifying assemblies during development and testing
• Experience in high-speed circuitry design such as DDR memory interfaces 
• Proficiency with CAD systems for schematic capture and experience in directing and reviewing PCB layout for signal integrity and EMI 
• FPGA design and debug experience
• Experience in debugging and design validation of microcontrollers or SoC-based systems  
• Experience creating and implementing software and hardware test benches
• Demonstrated proficiency analog circuit design, analysis, and simulation / modeling 
• Strong communication and collaboration skills, presenting design ideas and receiving input from internal customers and product marketing
• Intel/Altera Quartusexperience and SystemVerilog proficiency is preferred 

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $139,000 to $152,000 depending on skills, competency, and the market demand for your expertise.

Position

Eikon Therapeutics is seeking its first Senior Director, SEC Reporting & SOX to lead and scale the company’s external reporting, internal controls and technical accounting. This highly visible role will set strategy, vision, and direction for SEC reporting, SOX compliance, and financial governance, translating company objectives into scalable, cross-functional execution. The Senior Director will serve as a trusted advisor to executive leadership, anticipating regulatory and market factors that may impact the company’s position over the long term. This role requires the ability to operate autonomously, make decisions with multi-year impact, and coordinate simultaneous initiatives across the organization.

About You

You are a strategic, hands-on leader with deep expertise in SEC reporting, SOX and technical accounting who thrives in evolving, high-growth environments. You are comfortable working with abstract concepts and ambiguity, and you translate complexity into clear strategy and execution. You bring sound judgment and understand that decisions in this role may have long-term implications for the company’s success. You are expected to partner with leaders cross-functionally and at varying levels within the company to better understand departmental operations and controls. You are a collaborative and influential partner who communicates with credibility and confidence, effectively engaging executive leadership and external stakeholders. You enjoy implementing systems, and scalable processes, and balance rigor and compliance with pragmatism appropriate to the company’s stage.

What You'll Do

• Lead the company’s SEC reporting strategy and execution, including preparation and review of Forms 10-K, 10-Q, 8-K, proxy statements and other required filings, ensuring accuracy, completeness, and timeliness.
• Coordinate with internal teams such as Legal, FP&A, and Stock Administration to collect required data for disclosures.
• Serve as a key point of contact for external auditors by providing support schedules, documentation, and responses during audits and reviews.
• Prepare and review external reporting components tied to the close process, including cash flow statements, equity, and share based compensation.
• Establish, implement, and continuously evolve a Sarbanes-Oxley (SOX) compliance framework, including risk assessment, control design, documentation, testing, remediation, and optimization as the company scales.
• Develop and implement company-wide policies, practices, and governance structures related to financial reporting and internal controls, ensuring alignment with regulatory requirements and business needs.
• Execute the company’s SOX compliance program and assist with conducting audits of select operational, information technology, and compliance processes in timely manner.
• Act as a strategic partner to executive leadership, providing insight, guidance, and influence on financial reporting, compliance, and risk management matters.
• Serve as a technical accounting expert – proactively evaluate complex transactions and provide technical accounting guidance and disclosure recommendations, ensuring compliance with US GAAP and SEC reporting requirements.
• Anticipate regulatory, operational, and organizational factors that could influence reporting strategy and company positioning, and proactively recommend solutions.
• Stay current on FASB and SEC pronouncements and interpret impact to the company in partnership with internal partners and external auditors and identify, research, and prepare technical memoranda for complex transactions.
• Partner cross-functionally with Accounting, FP&A, Legal, IT, Internal Audit, and external auditors and advisors to ensure cohesive execution and shared ownership of outcomes.
• Lead, mentor, and develop the SEC reporting and SOX organization, directly or through subordinate leaders, fostering high performance and continuous improvement.
• Oversee external audit relationships and third-party advisors, ensuring effective coordination and high-quality deliverables.
• Drive initiatives that solve company-wide, cross-functional challenges, balancing speed, accuracy, and long-term sustainability.

Qualifications

• Bachelor's degree with 15+ years of experience or a post-graduate degree in Finance and Accounting.
• 12+ years of experience in public accounting and/or related industry experience.
• 6+ years with a technical accounting focus; deep technical proficiency across various areas of US GAAP and ability to research independently.
• Extensive experience leading SEC reporting and SOX compliance in a public or recently public company; biotech or life sciences experience strongly preferred.
• Proven track record of working with abstract, complex issues and translating them into actionable strategy and execution.
• Strong understanding of US GAAP, SEC regulations, SOX, and internal control frameworks.
• Experience building and scaling teams, systems, and processes in high-growth, evolving environments.
• Exceptional communication, influence, and negotiation skills, with the ability to partner effectively with executive leadership and external stakeholders.
• Sound judgment and decision-making skills, recognizing that actions and recommendations may have long-term impact on the company’s success.
• Experience with SAP S4/Hana and ActiveDisclosure preferred.
• CPA, CIA or similar certification preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $235,000 to $256,500 depending on skills, competency, and the market demand for your expertise.

Position

As a Senior Medical Writer 2, you will play a pivotal role in translating complex scientific and medical information into clear and concise written materials. Operating in a dynamic and collaborative environment, you will contribute to the development of various documents that support our research, clinical trials, and regulatory activities.

About You 

The ideal candidate for this position should possess strong writing and communication skills, with the ability to effectively convey complex scientific concepts in a clear and concise manner. Exceptional attention to detail and a commitment to producing accurate and high-quality written materials are essential. Proficiency in Microsoft Office Suite and familiarity with scientific writing tools is important, and the candidate should be capable of thriving in a fast-paced and collaborative work environment. While knowledge of clinical research, regulatory requirements, and biotechnology is advantageous, it is not required.

What You’ll Do

• Document Preparation: Create a wide range of medical and scientific documents, including clinical study protocols, investigator brochures, regulatory submissions, and scientific publications.
• Content Development: Collaborate closely with cross-functional teams to collect and interpret data, ensuring accuracy and relevance in written materials.
• Regulatory Compliance: Ensure that all written materials strictly adhere to regulatory guidelines, industry standards, and internal quality standards.
• Literature Review: Conduct comprehensive literature reviews to support the development of evidence-based documents.
• Data Interpretation: Proficiently interpret and summarize complex scientific data and clinical trial results for various audiences.
• Editing and Proofreading: Review and edit documents for grammar, clarity, and consistency while maintaining a high level of accuracy.
• Collaboration: Collaborate closely with scientists, clinical teams, and regulatory affairs professionals to align written materials with project goals and timelines.
• Mentorship: Provide guidance and mentorship to junior medical writers, fostering their professional growth and development.

Qualifications

• PhD with 3 years of experience or a Master’s degree with 6 years of experience or a Bachelor's degree with 8 years of experience in a relevant field (e.g., life sciences, healthcare, or related discipline). 
• Strong writing and communication skills, with the ability to effectively convey complex scientific concepts in a clear and concise manner.
• Must have hands on experience with independently drafting CSRs, ICFs, IBs, Protocols, and/or CTD modules
• Exceptional attention to detail and commitment to producing accurate and high-quality written materials.
• Proficiency in Microsoft Office Suite and familiarity with scientific writing tools.
• Capability to thrive in a fast-paced and collaborative work environment.
• Knowledge of clinical research, regulatory requirements, and biotechnology is advantageous but not required.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $148,000 to $161,500 depending on skills, competency, and the market demand for your expertise.

Position

We are currently seeking an experienced leader for the clinical operations role of Director Clinical Study Management & Operational Excellence within Clinical Study Management.  The Director will manage all aspects of clinical operations study management, for assigned Eikon clinical programs, and be responsible for exquisite inhouse execution of all interventional clinical trials and oversight of requisite clinical vendors. The role will also support the systematic pursuit of optimal performance, efficiency, and quality across all aspects of clinical study management via a focus on operational excellence. Adherence to Good Clinical Practice (GCP), local and global policies and procedures to conduct high quality, inspection ready studies is essential. The Director is responsible for trial quality and audit responses and completion of CAPAs. They will be a single point of contact for managing clinical trial operationally excellent execution in all its aspects across clinical study phases. The position has multiple stakeholder touch points within Clinical Research & Development (CR&D) staff and important interactions with, inter alia, Quality Assurance (QA), Finance, Regulatory, Clinical Supplies, Business Development and Legal in a matrix-based organization.

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City, New Jersey or Millbrae, California offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth and collaboration.

About You

You are agile of mind, systematic, and a collaborative leader with global oncology clinical development experience and a passion for operational excellence and advancing patient care. You possess a deep understanding of clinical trial regulations, guideline, and the principles of GCP, ensuring compliance throughout the clinical trial process.

What You’ll Do

• In collaboration with senior clinical operations management, build and lead inhouse clinical operations study management teams responsible for operationally excellent delivery of assigned clinical protocols and programs.
• Manage clinical study management personnel across assigned clinical protocols and programs.
• Ensure that compliance, quality and timeline objectives are met for all assigned trials.
• Work collaboratively in a matrix organization with all internal stakeholders to deliver company clinical trial objectives on time, on budget and with high quality.
• Work with the CR&D Functional Area (FA) leads, as appropriate, in site management to accelerate enrollment and drive high quality.
• Take responsibility for any assigned clinical trial audits, working closely with the Clinical Quality Assurance group.
• Represent Clinical Study Management in operational excellence initiatives, in the systematic pursuit of optimal performance, efficiency, and quality across all aspects of clinical trial management and execution. Key components of operational excellence, in clinical study management, are: (1) quality and compliance, (2) process optimization, (3) technology integration, (4) risk management, (5) performance metrics, (6) cross-functional collaboration.
• Effectively solve problems and use judgment relating to national and international regulations, guidelines, investigator interactions and timelines.
• Effectively manage resources to ensure appropriately skilled and high performing staff members are assigned to support the effective execution of the portfolio and achieve CR&D objectives.
• Responsible for ensuring appropriate scientific and operational training for staff members.
• Serve as a talent magnet and develop, coach, and retain top talent in the clinical program team.
• Sets clear performance standards and holds self and organization accountable for achieving results with flawless execution.
• Embrace metrics and performance standards (KPIs) to drive continuous improvement in execution.

Qualifications

• A post-graduate degree with 12+ years of relevant experience with a Bachelor’s degree or 10+ years of relevant experience with a Master's Degree with a demonstrated working experience in clinical study management within the biotechnology, pharmaceutical, or healthcare industry. 
• Significant experience managing international clinical studies and programs in oncology.
• Proven track record of contribution to and delivery of clinical trials that support global regulatory submissions, clean regulatory inspections and product approvals or marketing authorizations.
• Significant management experience in a clinical trial setting with the ability to service and collaborate with different CR&D stakeholders in a matrix organization.
• Demonstrated situational leadership, independence, problem solving abilities, self-motivation, resourcefulness and ability to work in a fast-paced team environment.
• Significant management expertise should cover management of budget, resources, headcount, processes (and controls), productivity, quality and project delivery.
• A complete understanding of ICH GCP and Global/Regional/Local regulatory requirements is required.
• Strong communication skills requiring proficiency in written and spoken English.
• The incumbent must be competent and effective in written and verbal communication.
• Strategic thinking and high emotional intelligence.
• Strong operational excellence mindset and experience.
• Strong leadership that will attract, motivate, inspire, develop and retain talented staff.
• In addition, leadership skills that enable and drive alignment with the goals, purpose and mission of our company.

The expected hourly range for this role is $108.65 to $118.75 depending on skills, competency, and the market demand for your expertise.

Position

The Clinical Program Manager, Oncology, Clinical Study Management, will plan and oversee the execution of clinical trials in oncology and other therapeutic areas, as needed. This role  works in close partnership with cross-functional teams to ensure studies are delivered on time and within budget, with a strong focus on quality,  operational excellence, and best-in-class clinical study management. The successful candidate will play a key role in driving study execution, managing risks, and enabling high-performance collaboration across functions and regions.

This role will require a minimum of 3 day a week of onsite presence (or more as business needs require) in either of our California or New Jersey offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration. 

About You

You are collaborative, solutions oriented, flexible and have global clinical operational experience, with a passion for excellence in advancing patient care in oncology or neuroscience.

What You’ll Do

• Develop and own the operational strategy, timelines, and operational plans for clinical trials, ensuring alignment with program objectives and overall business goals.
• Oversee and lead cross-functional clinical trial execution, leading proactive risk identification, assessment, management, and driving alignment on mitigation strategies.
• Ensure high standards of quality by overseeing that clinical studies are conducted in accordance with approved protocols, company SOPs, applicable regulations, and maintain ongoing inspection readiness across the program lifecycle.
• Serve as central point of contact to facilitate cross functional team effectiveness, drive operational efficiency, and provide clear direction and guidance to ensure successful study execution.
• Work with minimal oversight from the Clinical Study Management Senior Director or Director, in collaboration with Clinical Study Management teams and Clinical Research and Development, Finance, and Legal functions.
• Oversee and manage vendor relationships and performance to ensure that clinical studies are completed in accordance with contractual specifications for quality, timelines, and cost.
• Provide regular, clear updates on study progress, risks, and mitigation plans to stakeholders and executive management (e.g., Clinical Study Management, Project & Portfolio Management, Clinical Research).
• Ensure that all study-related documents are accurate, complete, and filed appropriately in all clinical (Veeva TMF), regulatory, safety and finance systems in a timely manner.
• Lead, manage, hire, develop, and mentor global and regional Clinical Study Management personnel.
• Contribute to improvement initiatives, operational excellence efforts, and cross-functional projects that add value to Eikon Therapeutics.

Qualifications

• Bachelor’s degree with 8 years, a Master’s degree with 6 years, or a PhD with 3 years of relevant experience in life sciences, healthcare, or related field preferred. 
• Fluency in English (strong reading, writing, and speaking skills with the ability to effectively communicate with colleagues and stakeholders at all levels) is required.
• In-depth knowledge of ICH-GCP, regulations, directives, and guidelines.
• Proficiency in clinical trial management systems (CTMS, RTSM (IRT), Veeva Vault suite) and electronic data capture (EDC) systems.
• Proven ability to manage clinical studies within timelines and budgets while maintaining high quality standards and patient safety.
• Strong leadership and communication skills, with a demonstrated ability to work collaboratively with cross-functional teams.
• Experience managing budgets, resources, processes and controls, productivity, quality, and project delivery.
• High sense of accountability and urgency to prioritize deliverables effectively.
• Growth mindset and ability to independently.
• PMP certification preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $157,000 to $171,000 depending on skills, competency, and the market demand for your expertise.

Position 

We are seeking a talented, experienced, and highly motivated Clinical Trial Manager (CTM) to join our oncology Clinical Operations team. This role will require onsite presence a minimum of 3 days a week in our Millbrae, CA or Jersey City, NJ office to ensure effective global clinical trial management. The candidate must have the ability to work independently, be an effective leader, and an engaged clinical study team member in a dynamic, fast-paced environment.  You will play a key role in contributing to high quality in-house clinical study management, ensuring compliance with regulatory guidelines, and contributing to planning, managing and the successful completion of global clinical studies. 

This position requires proficiency in Mandarin, Cantonese, Japanese, or Korean and English (strong reading, writing, and speaking skills and an ability to effectively communicate with colleagues and stakeholders at all levels). 

About You 

You have strong communication skills and are a collaborative, agile, detail oriented trial leader with global trial experience, and you have a passion for operational excellence and advancing patient care for grievous diseases. 

What You’ll Do 

• In partnership with Clinical Study Management, provide guidance and daily oversight for the successful in-house management of all aspects of international in-sourced clinical trials, delivering high quality study data, on time and on budget 
• Develop and execute operational plans for the successful in-house implementation and management of oncology clinical trials 
• Collaborate with cross-functional teams, including data management, clinical scientists, regulatory and investigators, to ensure operational excellence and rapid delivery of high quality data. Ability to examine functional issues from a broader organizational perspective. 
• Manage all aspects of trial start-up activities, collaborating with other Clinical Operations functions (Site Engagement & Monitoring Excellence, and Supplier Relationship Management & Performance), to deliver efficient and effective site selection, feasibility assessments, and preparation of study-related documentation 
• Collaborate with other Clinical Operations functions (Site Engagement & Monitoring Excellence) to efficiently and effectively deliver study site initiation, training, and monitoring activities to ensure adherence to study protocols, regulatory requirements, and ICH-GCP guidelines 
• Collaborate with other Clinical Operations functions (Site Engagement & Monitoring Excellence) to develop and maintain strong relationships with investigators, study coordinators, and study site personnel to facilitate patient recruitment and retention 
• Monitor and evaluate study progress, identifying risks, issues, and deviations, and implement appropriate corrective actions to maintain study integrity and timelines 
• Ensure compliance with regulatory requirements, including ICH-GCP, FDA guidelines, and other applicable regulations throughout the trial lifecycle 
• As required, collaborate with external vendors, including CROs, central laboratories, and imaging providers, to ensure their efficient and effective deliverables to the trial 
• Contribute to the development and review of study-related documents, such as protocols, informed consent forms, case report forms (CRFs), and standard operating procedures (SOPs) 
• Prepare study materials and establish procedures to ensure adherence to study protocols and administrative requirements 
• Lead the creation and maintenance of all study files, including the study master file, and oversight of site files  
• Lead periodic review of the Sponsor Trial Master File

Qualifications 

• PhD and 3 years of relevant experience, or Masters Degree and 6 years of relevant experience, or Bachelors Degree and 8 years of relevant experience  
• Proven experience in Clinical Operations; Oncology trial management experience preferred 
• In-depth knowledge of clinical trial regulations, guidelines, and best practices, including ICH-GCP and FDA requirements, specific to oncology research 
• Demonstrated experience in managing and executing clinical trials from start-up to closeout 
• Strong project management skills, with the ability to effectively prioritize tasks, allocate resources, and manage study timelines and budgets 
• Excellent interpersonal and communication skills, with the ability to collaborate effectively with stakeholders at all levels, and create a clear sense of direction as necessary 
• Detail oriented with strong analytical and problem-solving abilities, capable of identifying and mitigating study risks and deviations 
• Proficiency in using Veeva clinical trial management systems (CTMS)  
• Understanding of oncology therapeutic areas, including familiarity with oncology treatment modalities, disease progression, and related medical terminology
• Ability to work onsite at least 3 days a week

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $130,000 to $142,500 depending on skills, competency, and the market demand for your expertise.

Position 

We are seeking a highly experienced, collaborative, and detail-oriented Contract Senior Manager capable of helping Eikon optimize its clinical Site Engagement and Monitoring function to support delivery of world class clinical drug development. The successful candidate will work closely with the Eikon Site Engagement and Monitoring Excellence (SEME) team, global Clinical Research Associates (CRAs) and internal study teams across therapeutic areas to oversee clinical site engagement and monitoring activities.

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our California or New Jersey offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.

About You

You have significant monitoring experience and a passion for leading, training, and mentoring CRAs. You are adept at developing and maintaining relationships with clinical trial sites and demonstrate the ability to oversee monitoring with a strong knowledge of Good Clinical Practice and clinical trial regulations to ensure subject safety, data integrity and inspection readiness. You have experience developing systems, resources, and tools to support high-quality monitoring and forecast CRA resourcing. You also have experience utilizing a Functional Service Provider (FSP) monitoring model embedded within a sponsor study team to execute major data collection and study milestones. You are a strong collaborator across clinical functional areas with a demonstrated ability to creatively and independently resolve complex issues that impact sites and CRAs.

What You’ll Do 

• Establish and foster effective relationships with internal and external stakeholders, such as the CRO and study team members.
• Promote awareness of Eikon’s clinical pipeline and programs to trial sites, investigators, and networks.
• Complete or oversee the qualification of sites and promptly facilitate site selection to support study milestone goals.
• Develop and maintain strong site relationships to support the site/patient experience and drive study team goals such as enrollment and major study milestones.
• Onboard and train CRAs to conduct high quality site qualification, initiation, and monitoring visits.
• Review and approve monitoring trip reports in the Clinical Trial Management System (CTMS).
• Perform and document monitoring oversight activities to assess monitoring quality and CRA performance.
• At times, perform the CRA role as needed, to support prompt site qualification, initiation, monitoring and close-out visits at key sites to meet urgent study milestones.
• Regularly review site and monitoring Key Risk Indicator (KRI) metrics to detect issues and ensure prompt resolution.
• Serve as an escalation point for CRAs and as a Subject Matter Expert (SME) to resolve site management and monitoring quality issues and develop/ensure implementation of Corrective and Preventive Action (CAPA) Plans as needed.
• Support CRAs to ensure sites are inspection-ready and support Eikon Clinical Quality Assurance during site inspections.
• Effectively utilize the CTMS and Trial Master File (TMF) to ensure SEME documents are promptly filed and site data is accurate.
• Contribute to monitoring process improvement initiatives by developing functional area Standard Operating Procedures (SOPs), Work Instructions (WIs), job aids, and tools.
• Contribute to improving site selection, monitoring, and monitoring oversight trip report templates in Veeva CTMS by identifying gaps, suggesting updates, testing and implementing change controls.

Qualifications

• 8+ years of experience with a Bachelor's degree, or 6+ years with a post graduate degree
• Experience utilizing Veeva CTMS and TMF is required.
• Experience supporting site and/or sponsor inspections is required.
• Working on-site from an Eikon office location (Jersey City, NJ or Millbrae, CA) 3 days per week is required during non-travel weeks.​

The expected hourly range for this role is $77.40 to $84.50 depending on skills, competency, and the market demand for your expertise.

Position

As a Clinical Trial Management Associate (CTMA), you will serve as a critical inhouse clinical operations partner in the execution, and oversight of Phase I–III global oncology clinical trials. Positioned between the Clinical Trial Associate (CTA) and Clinical Trial Manager (CTM), the CTMA brings increased ownership, autonomy, and judgment to the execution of clinical studies. You will independently manage assigned study responsibilities and help ensure the delivery of high-quality, compliant, and timely trial data in support of our mission to bring transformative therapies to patients.

This role requires a minimum of 3 days per week onsite (or more, as business needs require) in either our Jersey City (NJ), or Millbrae (CA) offices.

This position requires fluency in one of the following languages due to the nature of site interactions in various regions in EMEA or LATAM: Portuguese, German, Italian, French, Polish. 

About You

You bring a strong operational mindset, an ability to work independently, and a flexible and collaborative spirit. You are looking to grow beyond a CTA role and take on more direct responsibility for study deliverables, bringing with you valuable clinical research experience and a strong passion to contribute meaningfully to drug development through consistent operational excellence.

What You’ll Do

• Proactively support Clinical Study Management team members in the day-to-day execution of global clinical trials, with increasing independence and accountability for specific study components. Collaborate closely with assigned global (gCSM)/regional Clinical Study Management (rCSM) teams, ensuring operational excellence throughout study execution.
• Manage and coordinate critical study activities with minimal oversight such as site communications, and maintenance of study timelines, risk logs, and action trackers.
• Lead the coordination and execution of site start-up assigned activities across multiple countries, working closely with regulatory, study start-up, and site engagement and monitoring excellence inhouse teams.
• Independently maintain and oversee trial master file (TMF) quality and completeness, in collaboration with TMF Operations, ensuring inspection readiness at all times.
• Draft, review, and manage study documents such as monitoring plans, training materials, and site communications under the guidance of the CTM.
• Track and reconcile investigational product (IP) and clinical supply/lab shipments, proactively flagging discrepancies and collaborating with supply chain to resolve issues.
• Support site level budget tracking invoice reconciliation, and vendor communications in partnership with Clinical Operations and Finance.
• Coordinate and contribute to key study meetings (e.g., team meetings, vendor meetings, investigator meetings), including agenda development, meeting facilitation, and action item follow-up.
• Monitor enrollment and site performance metrics, contributing to analysis and mitigation strategies to meet enrollment goals and drive operational excellence.
• Partner with data manager lead to ensure timely site follow up (assigned sites) for query reconciliation to meet the study milestones (e.g., interim analyses goals, etc.).
• Ensure compliance with study protocols, SOPs, and regulatory guidelines (e.g., ICH-GCP, FDA) across all operational activities.

Qualifications

• Bachelor’s degree with 3+ years of relevant clinical trial experience or a Master’s degree with 1–2 years of experience.
• Demonstrated ability to work independently and manage multiple competing priorities with minimal oversight.
• Strong understanding of clinical trial processes and regulatory requirements (ICH-GCP, FDA).
• Experience using clinical systems such as CTMS, EDC, and eTMF; Veeva Vault experience is a plus.
• Excellent organizational and time management skills with high attention to detail.
• Strong written and verbal communication skills and ability to interact confidently with internal stakeholders and external partners.
• Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint, Project).
• Previous oncology trial experience preferred but not required.
• Working experience in LATAM/EMEA

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $122,000 to $133,000 depending on skills, competency, and the market demand for your expertise.

Position

We are seeking an experienced Associate Director, Investor Relations to help shape and execute our investor relations strategy during a critical phase of growth as a public, clinical-stage biopharmaceutical company. In this role, you will be responsible for supporting clear, consistent, and compliant communication with the investment community, while partnering closely with executive leadership, Finance, Scientific Affairs and Legal. You will play a hands-on role in preparing external messaging, supporting earnings and investor events, and managing investor-facing materials that accurately reflect company performance, pipeline progress, and long-term strategy. This position requires strong judgment, attention to detail, and the ability to operate effectively in a fast-paced, highly visible environment.

About You

You are a seasoned investor relations professional with experience supporting public-company communications, ideally within the biotechnology or life sciences sector. You are comfortable operating as a senior individual contributor, balancing strategic thinking with hands-on execution. You bring strong financial acumen, exceptional written and verbal communication skills, and the ability to distill complex scientific and financial information into clear, compelling narratives for diverse external audiences. You thrive in cross-functional environments, lead through influence, and exercise sound judgment when navigating sensitive, time-critical information.

What You’ll Do

• Partner with the CFO, CEO & Board Chair, and executive leadership to support the company’s investor relations strategy and ensure clear, consistent, and compliant communication with the investment community.
• Prepare and maintain high-quality investor-facing materials, including earnings presentations, investor decks, fact sheets, talking points, and Q&A documents that accurately reflect company performance, pipeline progress, and long-term strategy.
• Support quarterly earnings cycles end-to-end, including message development, script drafting, coordination of internal reviews, and post-earnings follow-up.
• Assist in planning and executing investor meetings, conferences, and non-deal roadshows, including preparation of executives and development of meeting materials.
• Serve as a key cross-functional partner to Finance, Legal, and Corporate Communications to ensure alignment across external messaging and adherence to disclosure and governance requirements.
• Monitor investor sentiment, analyst feedback, and peer activity; synthesize insights and provide thoughtful input to internal stakeholders.
• Help ensure all investor communications comply with SEC regulations, Reg FD, and internal disclosure controls.

Qualifications

• Post-graduate degree with 8+ years of experience, or a Bachelor’s degree with 10+ years of experience in investor relations, corporate finance, equity research, investment banking, or a related field.
• Prior experience supporting a public company in the biotechnology, pharmaceuticals, or life sciences sectors. Ideally a large cap company.
• Strong understanding of financial statements, capital markets, and investor expectations.
• Demonstrated ability to craft clear, concise, and compliant investor communications.
• Excellent written and verbal communication skills, with confidence interacting with senior executives and external stakeholders.
• High attention to detail, strong judgment, and the ability to manage multiple priorities under tight timelines.
• Ability to thrive in a dynamic, high-growth environment and operate effectively as an individual contributor.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $177,000 to $193,800 depending on skills, competency, and the market demand for your expertise.

Position

The Director, High-Throughput Biology (HTB) is responsible for the strategy, performance, and evolution of Eikon’s high-throughput screening and discovery platforms. This role leads end-to-end high-throughput screening execution across automated and imaging-based platform technologies, ensuring delivery of scalable, reproducible, decision-enabling data that supports portfolio priorities. Operating at the intersection of biology, automation engineering, and computational science, this leader establishes standards for assay robustness, data quality, platform reliability, and technical execution, while building a high-performing organization capable of advancing discovery programs efficiently and at scale.

About You

You are a strategic and technically grounded leader who brings deep expertise in high-throughput screening and platform biology, along with the ability to lead across biology, automation, and computational disciplines. You are comfortable operating at both the strategic and technical level, balancing organizational leadership with hands-on scientific engagement where needed. You bring strong judgment, cross-functional leadership, and a commitment to building scalable, resilient systems that support high-quality discovery execution. You are also experienced in developing teams, strengthening technical depth, and creating shared ownership across critical workflows and capabilities.

What You'll Do

• Set the vision and operating model for HTB, defining strategy, success metrics, and standards that ensure sustainable, reliable, high-quality screening data delivery across the portfolio.
• Partner cross-functionally at the assay-to-screening interface to align assay readiness, screening feasibility, platform capabilities, and project priorities.
• Lead high-throughput screening strategy and execution, partnering with HTB scientists and program leadership to drive prioritization, ensure feasibility, and enable data-driven decisions.
• Optimize team resourcing and representation to support screening design, execution, analysis, and program engagement across scientists and SRAs.
• Lead an integrated platform organization that aligns biology, automation, and data analytics into a cohesive screening engine, including workflows, robotics integration, quality control, reporting, and data practices.
• Build, develop, and retain a high-performing team through clear accountability, coaching, and development of technical and cross-functional capability.
• Provide hands-on technical leadership by shaping assay strategy, screening design, analytical methods, and data or automation tooling where needed.
• Establish scalable practices through documentation, playbooks, and shared ownership of critical workflows and code to strengthen continuity and reduce single-point dependency.

Qualifications

• PhD in Biological Sciences, Computational Sciences, or a related discipline with 10+ years of experience in high-throughput or high-content screening environments.
• Demonstrated expertise with automated screening platforms, including 384- and/or 1536-well formats.
• Experience screening compound libraries larger than 100k.
• Experience advancing drug discovery programs from hit identification through lead optimization.
• Experience with microscopy-based or imaging-enabled screening platforms.
• Experience with genetic screens or systems biology approaches.
• Strong expertise in statistical analysis and large-scale dataset quality control, with proficiency in Python.
• Experience building or contributing to scalable data processing pipelines.
• Proficiency with compound databases, LIMS, and enterprise data systems.
• Proven cross-functional leadership across biology, chemistry, engineering, and data teams.
• Experience with single-molecule imaging technology is preferred.
• Experience with novel technologies or assay development for drug discovery is preferred.
• Strong computational science capability and familiarity with machine learning or artificial intelligence applications in phenotypic or multiparametric screening are preferred.
• Demonstrated ability to build hybrid biology and computational teams is preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $213,000 to $232,750 depending on skills, competency, and the market demand for your expertise.

Position

We are currently seeking an experienced informatics engineer to contribute to the design, implementation, and development of our informatics processes and systems to support all phases of our research pipelines. You will work closely with our scientists and engineers to capture and manage functional requirements. You will be a core member of a team that is responsible to build scalable solutions to fulfill these requirements that fit into our information ecosystem and ensure the integrity of our data architecture.

About You

You are agile of mind and effectively communicate difficult concepts. You work well within a fast-paced, mission-driven, dynamic environment. You are prepared to tackle a broad selection of challenges as the company grows, and possess a deep desire to pursue creative solutions with broad guidance and a high degree of independence. You can partner with R&D leadership and functional area scientists to proactively identify areas of need, design solutions, prioritize work, coordinate pilot studies, ensure appropriate system usage, and regularly report on system metrics and portfolio execution.

What You'll Do

• Actively involved in the administration and integration of LIMS software and AI/ML platform into R&D projects and systems.
• Contribute to the design, development, test, and implementation of informatics solutions including LIMS, ELN, Inventory Management, etc.
• Implement data warehouse / data lake systems and pipelines for advanced analytics and AI/ML strategy .
• Implement data automation pipelines and ETL processes.
• Collaborate with a cross-functional team to develop an end-to-end digital architecture roadmap.
• Work with project stakeholders to analyze data management, analytics, and visualizations needs across R&D functions.
• Gather user stories, design applications, implement and integrate systems and guide the functionality of IT systems across the company.
• Ensure that systems are fully documented with system requirements, architectural design, and operational plans.
• Coordinate the training and support of end-users on system usage and best practices.
• Responsible for application licenses and forecasting annual usage.
• Participate in design of enterprise-wide data platform architecture and ensure the systems adhere to that architecture.
• Stay up-to-date with emerging technologies and trends in LIMS engineering and ML Platform.

Qualifications

• Bachelor’s degree with 5 years of relevant experience or a Master’s degree with 3 years of relevant experience in computer science, life science, engineering, or a related field or equivalent training, fellowship, and/or work experience.
• Experience with ELN, LIMS, scientific data management, compound registration, sample inventory, instrument data capture, assay results, and electronic laboratory notebooks, such as CDD Vault and Dotmatics.
• A track record of achievements in designing and implementing LIMS apps for data access and/or visualization.
• Experience in evaluating, configuring, and tuning LIMS software for customized needs.
• Experience with administration, implementation, and integration of AI/ML and Data Lake Platform, such as Databricks.
• Applicable experience in software development and/or systems integration, preferably within a scientific or laboratory environment, especially one that is related to drug development.
• Experience with programming, scripting, and query languages and platforms like Python, Java, JavaScript, SQL.
• Experience with different types of data storage implementations, relational and non-relational (e.g. key-value, document, SQL, graph/graph databases), and optimizations of data storage by mixing and matches.
• Familiarity with Docker, containerized applications, and AWS cloud computing services.
• Experience in documenting detailed software requirements, user stories, business processes, and/or software specifications for both custom and Commercial-Off-The-Shelf (COTS) systems.
• Familiarity with laboratory operations and workflows, experience with designing, implementing, and maintaining computational workflows involving multiple modular steps, and knowledge of data analysis in life sciences.
• Proven experience working closely with scientific stakeholders to understand their informatics needs, and subsequently defining complex system requirements, scope, objectives, and key results in the context of larger organizational goals.
• Excellent problem-solving and analytical skills in a fast-paced R&D environment where the product requirements and internal software tools may change over time.
• Able to present your work, both verbally and in writing, to diverse audiences including scientific stakeholders, technical teams, as well as research leadership.
• Experience working in a life sciences or biopharmaceutical environment such as early-stage research, drug discovery, or other biological sciences discipline is preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $134,000 to $146,300 depending on skills, competency, and the market demand for your expertise.

Position: 

The Associate Director, Clinical Data Analytics and Reporting is a leader responsible for establishing and scaling a Clinical Research & Development clinical analytics function for a growing biotechnology company. This role will define the analytics strategy, operating model, and technology roadmap, including the technical implementation to enable high-quality, data-driven decision-making across Clinical Research & Development, with primary focus on oncology programs.  This is a hands-on role requiring demonstrated expertise in design, development, test and support of complete analytics & reporting system lifecycle. This leader will partner closely with Clinical Operations, Biostatistics, Data Management, Clinical Research, Regulatory, Safety and Clinical Quality Assurance to ensure proactive risk identification, operational excellence, inspection-ready execution across the portfolio. 

About You 

The successful candidate will combine deep clinical development expertise with advanced analytics, data governance, and visualization capabilities. The ideal candidate for this role should possess a proven track record of designing, implementing and supporting end-to-end data analytics solutions using current state-of-the-art technologies, and a deep knowledge of emerging trends and best practices in data analytics.  

What will you do: 

• Collaborate with Stakeholders in different areas of Clinical Development R&D organization, IT System Owners and external vendors to define and implement the clinical analytics vision, strategy and capabilities (e.g., dashboard, etc.) aligned with clinical development objectives. 
• Establish a scalable analytics operating model suitable for early stage through late phase development.
• Translate complex clinical and operational data into clear, actionable insights for executive and study teams (including predictive and prescriptive analytics to anticipate risks and optimize trial execution).
• Design, development, test and deployment of the complete end-to-end analytics solution to enable decision-grade dashboards and metrics across Clinical R&D.
• Design and implementation of datawarehouse/datalake/lakehouse including star schemas.
• Collaborate with System Owners, Business Owners and Subject Matter Experts to map sources system objects and attributes to data warehouse objects.
• Develop, test and support data pipelines for extract, transform, load (ETL) of the source system data to populate datawarehouse/datalake/lakehouse.
• Develop end user facing dashboards and analytics solutions.
• Support the operations of the IT systems landscape ensuring system uptime, ETL and other job completion as per schedule, ongoing system changes and enhancements. 

Qualifications 

• Post Graduate degree with 8+ years of experience or a Bachelor’s degree with 10+ years of experience in development and support of Clinical Operations analytics solutions.
• Demonstrated strong experience working with developing end user dashboards using solutions such as Qlik, Power BI, Shiny R/Python.
• Strong Experience developing datalake/lakehouse solutions on platforms such as Snowflake, Databricks, AWS, and Azure.
• Strong working knowledge of development and management of database technologies such as Postgres, SQLServer etc.
• Experience with development of data pipelines including ETL from source systems to datawarehouse/datalakes/lakehouse using solutions such as Apache Airflow, Fivetran, dbt etc.
• Excellent oral and written communication skills with high EQ to effectively collaborate with business cross-functional teams.
• Understanding of the clinical development lifecycle and demonstrated experience building analytics capabilities in clinical development
• Knowledge of Report/Dashboard development in Veeva R&D Vaults such Clinical, RIM, Quality, Safety is preferred.
• Knowledge of IT Computer System Validation (CSV) in a GxP environment is preferred.
• Experience with Automation and AI Agent Frameworks is preferred.
• Deep knowledge of RBQM, Quality by Design (QbD) and regulatory/operational expectations for clinical oversight is preferred. 

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $191,000 to $209,000 depending on skills, competency, and the market demand for your expertise.

Position

The Associate Director, Clinical Study Management, will be responsible for overseeing the execution of clinical trials in oncology and other therapeutic areas, as required. The successful candidate will work closely with cross-functional Clinical Research & Development teams to ensure successful completion of studies within timelines and budget, with a focus on exquisite quality to support operational excellence and world class inhouse clinical study management.

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our California or New Jersey offices to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.

About You

You are collaborative, solutions oriented, flexible and have global clinical operational experience, with a passion for excellence in advancing patient care in oncology.

What You’ll Do

• Team leader and builder, who manages clinical trial deliverables, timelines, and budgets per the Clinical Development and Operational Plans
• Works with minimal oversight from the Clinical Operations Senior Director or Director, in collaboration with Clinical Study Management teams and Clinical Research and Development functional teams
• Demonstrate broad understanding of therapeutic and clinical drug development expertise to influence study design and program-level decisions 
• Provide direction to cross-functional study teams to ensure successful study execution Ensure that clinical studies are conducted  following approved protocols, FDA Regulations, ICH-GCP, EMA, PMDA, other relevant regulations, directives, and guidelines, and company procedures and quality documents
• Oversee risk identification, assessment, and mitigation strategies to ensure patient safety and data integrity
• Responsible for the implementation of processes and systems that will facilitate inspection readiness throughout the lifecycle of the trial.
• Oversee the preparation and maintenance of detailed clinical trial project timelines
• Manage ancillary (non CRO) vendor relationships and performance to ensure that clinical studies are completed following contract specifications of time, cost and quality.
• Work with finance, legal, and external vendors to ensure the assigned studies are meeting the target milestones
• Provide regular updates on study progress to stakeholders (e.g., Clinical Operations, Project & Portfolio Management, Clinical Research)
• Ensure that all study-related documents are accurate, complete, timely and filed appropriately in all clinical (Veeva TMF), regulatory, safety and finance systems.
• Responsible for hiring, performance management, career development, and providing mentorship to Clinical Study Management personnel.
• Contribute to initiatives and projects adding value to Eikon Therapeutics

Qualifications

• Minimum of 10 years of related experience with a Bachelor’s degree or 8 years and a post-graduate degree.
• Experience leading large, global clinical trials, preferably in oncology
• In-depth knowledge of ICH-GCP, EMA guidelines and other relevant regulations and guidelines.
• Proven ability to manage clinical studies within timelines and budgets while maintaining high quality standards and patient safety.
• Strong leadership and communication skills, with a demonstrated ability to work collaboratively with cross-functional teams.
• Experience with management of the budget, resources, headcount, processes and controls, productivity, quality and project delivery.
• High sense of accountability and urgency to prioritize deliverables.
• Growth mindset and capable of working independently.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $183,000 to $199,500 depending on skills, competency, and the market demand for your expertise.

Position

Eikon is seeking a senior scientist to join its Advanced Imaging Research group, a multidisciplinary team of experimental and computational scientists focused on understanding and improving the capabilities of Eikon’s imaging platform. This person would execute experiments and interpret them by performing novel computational analysis and is ideal for a scientist who can combine deep analytical rigor with the practical understanding of executing high quality single molecule experiments. As a Senior Scientist, you will apply analytical methods to extract biological insight from your large-scale single molecule imaging datasets, while also partnering on experimental design, assay evaluation, and technology development. You will help determine how Eikon’s tools can be applied to new targets, new biological questions, and new technology areas that expand the impact of our platform in drug discovery applications.

About You

You are a scientifically curious scientist who enjoys using quantitative imaging and computational approaches to solve difficult biological problems. You are equally comfortable at the bench and at the command line, and you can navigate technical challenges across domains. You have a proven track record of building and thoughtfully applying new methods to gain deeper insight into a biological system, especially in imaging-based modalities. You are a strong communicator, comfortable engaging experts from other disciplines and working together to solve tough problems. You see the enduring value of bringing together scientific and engineering leaders to address grievous human illness.

What You’ll Do

• Work with single molecule imaging data at an unprecedented scale, using protein motion to derive biological insights.
• Become a champion of Eikon’s platform, leading technology development efforts to open new opportunities in drug discovery and development.
• Collaboratively plan, design, conduct and analyze experiments with experts in oncology, neurobiology, machine learning, image processing, analytical modeling, chemistry, hardware engineering, and more.
• Serve as a scientific resource to peers and collaborators by sharing best practices, supporting training, and helping others design interpretable experiments and analyses.
• Act as a functional expert to project teams and clearly communicate results and next steps to lead the team through development and use of single molecule experiments.

Qualifications

• PhD or equivalent experience in biophysics, molecular biology, cell biology, or related field with 5+ years of post-graduate research experience.
• Demonstrated expertise in quantitative single molecule imaging techniques such as single particle tracking, STORM/PALM, or single molecule fluorescence in situ hybridization, or spatial genomics.
• Experience with scientific Python and working with large, image-derived datasets.
• Demonstrated ability to independently design, execute, and communicate results of complex experiments that support collaborative work.
• Experience in principled method and/or workflow development.
• Previous drug discovery experience is strongly preferred.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $143,000 to $156,750 depending on skills, competency, and the market demand for your expertise.

Position

We are seeking a dynamic and experienced Senior Director, Information Security to lead our cybersecurity and compliance efforts. Reporting directly to the Vice President, Information Technology the successful candidate will play a pivotal role in safeguarding our sensitive data, protecting our digital assets, and ensuring regulatory compliance across all aspects of our operations. 

About You

The ideal candidate is an accomplished cybersecurity leader with a strong track record in information security management. They possess extensive knowledge of cybersecurity technologies, including network security and threat detection. With exceptional problem-solving and decision-making abilities, they are well-equipped to lead the development and execution of a comprehensive information security strategy while fostering a culture of collaboration and security awareness among employees. 

What You'll Do

• Develop and execute a comprehensive information security strategy aligned with business objectives, regulatory requirements, and industry best practices. 
• Oversee the implementation and maintenance of robust cybersecurity measures, including but not limited to network security, endpoint protection, data encryption, access controls, and incident response protocols.
• Lead the development and enforcement of information security policies, procedures, and standards to mitigate risks and protect against cyber threats.
• Collaborate with cross-functional teams to integrate security into the design, development, and deployment of new products and technologies.
• Provide strategic guidance and direction on compliance initiatives, ensuring adherence to relevant regulations such as HIPAA, GDPR, FDA guidelines, and other global data protection laws.
• Conduct regular risk assessments and security audits to identify vulnerabilities, assess the effectiveness of controls, and recommend remediation actions as needed.
• Foster a culture of security awareness and compliance throughout the organization through training, communication, and employee engagement initiatives.
• Ensure that security policies and standards are understood and applied in contracts, engineering projects, and infrastructure.
• Serve as the primary point of contact for security incidents, breaches, and regulatory inquiries, leading investigations and coordinating response efforts as necessary.
• Collaborate closely with Cyber SOC for incidence response.
• Stay abreast of emerging threats, trends, and technologies in the cybersecurity landscape, continuously evaluating and enhancing the company's security posture.
• Represent the company in discussions with regulators, industry partners, and stakeholders on matters related to information security and compliance. 

Qualifications

• Post Graduate degree with 12+ years of experience or a Bachelor's degree with 15+ years of relevant experience.  
• Strong communication skills with the ability to manage up, down and to the sides. 
• Extensive knowledge of regulatory requirements and compliance standards relevant to the biotech and healthcare industries, such as HIPAA, GDPR, FDA regulations, etc. 
• Proven track record of designing and implementing effective cybersecurity programs, including risk management, threat detection, and incident response. 
• Excellent leadership, communication, and interpersonal skills, with the ability to influence and collaborate across all levels of the organization. 
• Commitment to diversity, equity, and inclusion, with a demonstrated ability to foster a culture of belonging and respect in the workplace. 
• Strong background in biotech, pharmaceuticals, or healthcare, with specific experience in global clinical trials preferred. 
• Relevant industry certifications (e.g., CISSP, CISM, CRISC) highly desirable. 

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $248,000 to $270,750 depending on skills, competency, and the market demand for your expertise.

Position

The Associate Director, CMC Drug Product will lead drug product development and clinical manufacturing activities across multiple programs, with a strong focus on early- to mid-stage small-molecule oral solid dose compounds. This individual will be responsible for defining and executing drug product strategies from preclinical development through clinical supply, while ensuring compliance with global regulatory requirements. In this role, you will serve as the primary drug product CMC lead, partnering closely with internal cross-functional teams and external CDMOs to advance the company’s pipeline. The ideal candidate brings deep technical expertise in formulation and process development, strong project leadership skills, and hands-on experience supporting regulatory submissions for early clinical programs.

About You

You are a drug product CMC leader with a strong foundation in pharmaceutical sciences and a proven track record advancing small-molecule oral solid dose programs in a fast-paced biotech environment. You are comfortable owning drug product strategy end-to-end, from preformulation and formulation development through clinical manufacturing and packaging, with particular strength in early-stage development. You thrive in cross-functional settings and are experienced working with CDMOs to deliver phase-appropriate formulations, leveraging solid dose processing technologies such as spray drying and compression. You bring a clear understanding of regulatory expectations for early and mid-stage programs and can translate technical development work into high-quality CMC documentation. You are hands-on when needed, detail-oriented, and proactive in identifying risks, driving solutions, and keeping programs on track.

What You’ll Do

• Lead the preclinical formulation development and drug product development from early clinical through commercial stages
• Oversee formulation development and scale-up activities at CDMOs
• Ensure robust and scalable manufacturing processes are in place  
• Collaborate with cross-functional teams including Research Project Teams, Regulatory Affairs, Quality Assurance, Manufacturing, Supply Chain and Clinical Operations to ensure seamless product development delivery
• Develop and execute project plans, timelines, and budgets
• Ensure all CMC activities comply with regulatory requirements (FDA, EMA, etc.)
• Prepare and review CMC sections of regulatory submissions, including INDs, NDAs, CTDs, etc.
• Interact with regulatory agencies to address CMC-related queries and provide necessary documentation 
• Mentor and develop junior staff members 
• Identify and manage external partners, including CMOs and CROs
• Ensure quality and timely delivery of contracted services
• Negotiate contracts and manage vendor performance 
• Potential to contribute to setting up new, in-house non-GMP formulation laboratory

Qualifications

• A Master’s degree in Pharmaceutics, Chemical Engineering, or a related field with 8+ years of experience in pharmaceutical formulation and drug product development, or a PhD with 6+ years of experience in pharmaceutical formulation and drug product development
• Experience with development of various dosage forms (solid oral, injectable, etc.) and different manufacturing processes (compression, SDD, etc.)
• Previous experience serving as a drug product lead though IND and/or NDA stages
• Proven track record of successful FIH formulation development and regulatory submissions
• Strong understanding of FDA and EMA regulatory requirements and quality systems
• Excellent communication, leadership, and problem-solving skills with hands-on knowledge of cGMPs and quality control processes 
• Ability to work in a fast-paced, dynamic environment and manage multiple priorities
• Excellent interpersonal and communication skills, capable of leading and motivating teams

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $174,000 to $190,000 depending on skills, competency, and the market demand for your expertise.

Position

The Lab Data Manager will be responsible for timely and high-quality management of local lab reference ranges supporting the Eikon portfolio including the loading of Lab Normal Ranges (LNR) within the EDC system and the management of LNR issue tracking and health status of a particular lab, site or study.

This role will require a minimum of 3 days a week of onsite presence (or more as business needs require) in either of our Jersey City, NJ office or our Millbrae, CA office to ensure effective management, operational excellence and high-performance delivery of clinical studies and to support the expected significant team growth & collaboration.

About You

You are a driven individual that focuses on detail.  An expert in data management and a strong collaborator.

What You’ll Do

• Review and quality control (QC) the reference ranges provided by the site or, if applicable, other Eikon functional groups.
• Create lab normal range import file and uploads it into EDC local lab module.
• Be responsible for LNR issue tracking and maintaining health status at lab, site, and study level for communication to Data Management leadership or other cross functional teams.
• Manage local lab range units within the EDC system including change control process.
• Collaborate with Data Management colleagues, other Eikon functions, and study site personnel to continuously improve the collection and loading of LNR data.
• Provide LNR training for Data Management and other Eikon functions as required.
• Be responsible for the creation and maintenance of any Data Management owned controlled documents and provide SME knowledge to any cross functional controlled documents related to LNRs.
• Act as the LNR SME for Health Authority inspections and audits.
• Serve as a primary point of contact for internal and external study team members regarding local lab reference ranges.
• Serve as a backup for medical coding activities.

Qualifications

• 6+ years of experience with a Bachelor's degree in a health related field (Chemistry, Nursing, etc.); or 4+ years of experience with a post graduate degree
• Proven experience in clinical data management gained from working at recognized clinical data management suppliers/vendors, reputable CRO(s) and/or a Sponsor environment working on multi-phase, multi-therapeutic (Oncology experience will be preferred) and diverse clinical trials from study initiation to completion and associated regulatory submission and inspection preparation.
• 3+ years of experience focused on the collection and maintenance of local lab reference ranges within standard clinical data management systems.
• Expertise with Lab analytes collected and tested in Oncology clinical trials is preferred.
• Able to work collaboratively on multi-disciplinary project teams and develop productive relationships with external vendors.
• Sound knowledge of Clinical Drug Development Process, FDA/ICH guidelines and industry standard practices regarding data management and local lab ranges.
• Strong knowledge and experience of EDC systems (Veeva CDMS preferred); demonstrated knowledge of Microsoft Office skills and well versed in industry trends and emerging technologies supporting data collection.
• Experience using a Local Lab Module within a standard EDC system is required.
• Strong project management, metrics analysis and reporting methodologies experience.
• Excellent oral and written communication skills and able to communicate effectively with senior management and cross-functional teams.
• Good knowledge of CDASH/CDISC (CDASH CRF Library implementation experience is preferred).
• Knowledge of submission requirements, [e.g. New Drug Application (NDA)/Biologics License Application (BLA)/Market Authorization Application (MAA)].
• Medical Coding experience is a plus.

At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:​

• 401k plan with company matching​
• Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)​
• Mental health and wellness benefits​
• Weeklong summer and winter holiday shutdowns​
• Generous paid time off and holiday policies​
• Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies ​
• Enhanced parental leave benefit​
• Daily subsidized lunch program when on-site​

The expected salary range for this role is $104,000 to $114,000 depending on skills, competency, and the market demand for your expertise.