Team Description:

The Preclinical Team is responsible for designing, conducting, documenting, analyzing, and reporting preclinical studies. Our team provides a means for ensuring the safe, effective, and robust implantation of Neuralink devices into animals and, ultimately, humans.

Job Description and Responsibilities:

The Study Coordinator provides critical operational and project management support to the Study Director in GLP-regulated preclinical studies for Neuralink devices. This role handles the majority of day-to-day coordination, scheduling, data compilation, and administrative tasks, enabling the Study Director to focus on scientific oversight, data interpretation, and regulatory compliance. The Study Coordinator acts as a key liaison across the preclinical team, technical staff, and cross-functional groups to ensure studies progress smoothly, on time, and in compliance with protocols and SOPs. The Study Coordinator will:

• Support the Study Director in developing study protocols, amendments, and related documentation.
• Facilitate cross-functional communication, establish and track study timelines, and prepare/lead study milestone meetings.
• Identify and help eliminate roadblocks that could delay study progress.
• Assist with implementation of test methods and practices described in the study protocol and SOPs.
• Help ensure all experimental data, including observations of unanticipated responses of the test system, are accurately recorded and verified.
• Manage the study schedule, alerting the Study Director and team to critical data collection points or deadlines.
• Support the documentation and addressing of self-reported or QAU-generated deviations that may affect study quality.
• Compile data, organize contributing scientist reports, and assist in preparing the final study report so it accurately reflects study results.
• Maintain organized study files, track communications, and support archiving of data, documentation, protocols, specimens, and reports per GLP.
• Coordinate day-to-day study activities with technical staff, veterinary teams, and external partners (e.g., CROs if applicable).
• Contribute to internal tracking systems, meeting minutes, and status updates for the Preclinical Team.

Required Qualifications:

• Bachelor’s degree  in biology, neuroscience, biomedical engineering, animal science, or a related field.
• Minimum 1 year of experience in preclinical research support, study coordination, or project management (academic experience applies).
• Solid understanding of GLP regulations (21 CFR Part 58), basic knowledge of ISO 10993, and familiarity with in vivo animal studies.
• Strong organizational and project management skills with proven ability to manage timelines and multiple priorities.
• Excellent attention to detail and proficiency in data compilation, documentation, and Microsoft Office (or equivalent) tools.
• Experience working in or supporting animal research facilities with IACUC protocols.

Preferred Qualifications:

• Master’s degree  in biology, neuroscience, biomedical engineering, animal science, or a related field.
• Direct experience with neural device implantation studies or neurosurgical models.
• Background in a CRO or medical device preclinical setting.
• Familiarity with electronic data capture systems or GLP-compliant documentation platforms.

Additional Requirements and Competencies:

• Willingness to work in an animal research facility environment (with required training and PPE).
• Flexibility in schedule to support critical study timepoints.

Team Description:

Join our innovative Equipment Quality Team, a dynamic collective of experts dedicated to maintaining the precision and efficacy of high-tech equipment in preclinical and manufacturing domains. Engage with the latest in biomedical devices, industrial instrumentation, and high-end technologies like lasers and RF systems. As pioneers who've crafted a robust equipment program from scratch, we champion creative problem-solving and strive to set industry benchmarks. Immerse yourself in a mission-critical role that propels safety and regulatory compliance to new heights, and become part of a collaborative force driving the future of biomedical quality.

Job Description and Responsibilities:

Neuralink is seeking an Equipment Quality Technician with a strong knowledge of applied metrology. This technician will calibrate, repair, and perform preventative maintenance on equipment in the quality program. In addition, they will troubleshoot and repair instruments and systems. This role requires participation in cross-functional teams and some travel. Additionally, you will be expected to:

• Calibrate and perform preventive maintenance on any instrument or device in the equipment quality program with little to no supervision
• Provide the technical expertise for assisting management in developing work procedures and protocols
• Assist in the design, fabrication, check-out, start-up, and acceptance of new or modified equipment
• Determine and requisition parts required for maintenance repairs
• Adhere to cGxP guidelines, SOPs, and safety rules/regulations
• Assist management with determining work schedules and project costs
• Work closely with cross-functional team members  in regards to continuous improvement activities, solving problems, and improving overall product quality
• Explain calibration issues and processes to equipment custodians and management

Required Qualifications:

• Ability to comprehend and apply manuals and schematics for maintenance and troubleshooting
• Proficiency in using hand tools, physical/dimensional test instruments, and electronic test instruments
• Able to work in a dynamic, fast-paced environment
• Strong interpersonal skills: ability to work with colleagues and cross-functional teams in a professional and organized manner
• Competence in operating computing hardware and standard software
• Minimum of 1 year of experience related industrial instrumentation/calibration experience and/or training; or equivalent combination of education and experience
• Willingness to assist with other Quality Engineering activities such as facilities, equipment, and facilities validation

Preferred Qualifications:

• Experience in PMEL, TMDE, Metrology, Calibration, Instrumentation, Validation, or Biomedical Equipment
• Associates or Bachelors Degree in Science, Technology, Engineering, Mathematics or military training in calibration
• Relevant experience working in a highly regulated (e.g., GMP, GCP, GLP) environments

Team Description:

The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what’s possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is critical  in translating Neuralink’s BCI technology for clinical use!

Job Description and Responsibilities:

As a Clinical Program Manager, you will be the primary architect of Neuralink’s human clinical trial operations, transforming high-level strategy into rigorous, executable clinical programs. We are seeking a high-autonomy leader who thrives on ambiguity and drives projects to completion with surgical precision. In our hyper-dynamic environment, you aren't just managing timelines—you are building the infrastructure for the future of neurotechnology. You will be expected to:

Strategic Oversight & Relationship Management

• Act as the Principal Lead for complex clinical programs, owning end-to-end delivery and ensuring all milestones align with broader organizational objectives.
• Cultivate High-Stakes Partnerships across internal engineering and regulatory teams, as well as external vendors, strategic partners, and world-class clinical research sites.
• Champion Stakeholder Readiness by overseeing the training and credentialing of cross-functional teams, ensuring every contributor is equipped to operate within the trial’s rigorous requirements.

Operational Excellence & Scalability

• Engineer Scalable Frameworks to expand clinical operations across diverse global geographies, prioritizing safety, quality, and regulatory compliance at every inflection point.
• Lead Commercial & Financial Negotiations with trial sites, driving contract execution, budget optimization, and long-term financial planning to maximize trial efficiency without compromising site engagement.
• Drive Data Intelligence by leading the synthesis and analysis of clinical data to provide actionable insights for program refinement.

Compliance & Regulatory Stewardship

• Navigate Global Regulatory Landscapes to secure study approvals and maintain impeccable standing with Institutional Review Boards (IRB), Research Ethics Committees (REC), and relevant governing bodies.
• Enforce Rigorous Quality Standards, maintaining an expert-level command of Good Clinical Practices (GCP), international regulatory requirements, and site-specific Standard Operating Procedures (SOPs).
• Foster a Culture of Accountability, proactively identifying operational risks and implementing mitigation strategies to ensure the integrity of the clinical program.

Required Qualifications: 

Strategic Leadership & Clinical Expertise

• Extensive Industry Tenure: 7+ years of progressive leadership experience in clinical research, specifically within Class III medical devices, neurology, or high-complexity life sciences.
• Clinical Architecture: Advanced proficiency in clinical study design, endpoint selection, and the development of robust data analysis plans for first-in-human or pivotal trials.
• Regulatory Mastery: Deep technical knowledge of Global Good Clinical Practice (GCP) and international regulatory standards (e.g., ISO 14155, MDR, FDA 21 CFR Part 812).

Data Intelligence & Analytical Rigor

• Quantitative Fluency: Professional experience leveraging statistical methods or programming languages (Python, R) to drive data-led decision-making and trial optimization.
• Complex Problem Solving: Proven track record of interpreting multi-dimensional datasets and translating complex scientific findings into executive-level strategy.
• Meticulous Precision: A high-level of organizational rigor with the ability to manage competing high-priority workstreams in a fast-paced, high-stakes environment.

Communication & Interdisciplinary Integration

• Cross-Functional Catalyst: Demonstrated success leading integration between neural engineering, clinical neurosurgery, and regulatory affairs to achieve unified program goals.
• Scientific Diplomacy: Exceptional written and verbal communication skills, with the ability to distill complex technical and clinical concepts for diverse audiences, from internal engineers to external ethics committees.
• Operational Autonomy: A self-starting leader who initiates critical workstreams independently and maintains a relentless focus on deadline accuracy and operational efficiency.

Mission-Critical Mindset

• High-Stakes Resilience: A documented history of thriving in high-pressure, rapidly evolving environments where pivots are frequent and the margin for error is razor-thin.
• Advocacy & Influence: Strong presence and "scientific diplomacy" skills, with the ability to represent Neuralink’s clinical vision to world-class neurosurgeons, key opinion leaders (KOLs), and global health authorities

Preferred Qualifications: 

Advanced Academic & Technical Background

• Advanced Degree: PhD, MD, or Master’s degree in a relevant field (e.g., Neuroscience, Biomedical Engineering, Clinical Research, or Biological Sciences).
• Neurotech Specialization: Direct experience managing clinical trials for Class III active implantable medical devices (AIMDs), specifically Brain-Computer Interfaces (BCI) or Neuromodulation systems.
• Computational Fluency: Advanced proficiency in Python or R for automated data visualization, clinical dashboarding, or sophisticated statistical modeling.

Strategic Clinical Leadership

• First-in-Human (FIH) Mastery: Proven success in leading Early Feasibility Studies (EFS) and navigating the unique safety and ethical rigors of pioneering human trials.
• Global Expansion Experience: Experience scaling clinical operations across international jurisdictions, including familiarity with O-US regulatory bodies and localized clinical trial infrastructure.
• Financial Stewardship: Demonstrated expertise in multi-million dollar budget management, including sophisticated resource allocation and vendor contract optimization.

Innovation & Process Design

• Clinical Systems Architecture: Experience implementing and optimizing Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), and eTMF platforms for high-growth environments.
• Agile Clinical Operations: Ability to apply "lean" or "agile" methodologies to clinical trial workflows, reducing cycle times while maintaining absolute compliance.
• Interdisciplinary Synthesis: A rare ability to translate high-level engineering specifications into clinical protocols that are both scientifically rigorous and operationally feasible for surgical teams.

Team Description:

The Neuralink Clinical team is at the heart of an ecosystem that merges neuroscience, engineering, and medicine. We work to shape the future of brain-computer interface (BCI) technology through the planning, launch, and execution of groundbreaking human clinical trials. Our team is built on a foundation of excellence, aiming to uphold the highest standards of Good Clinical Practice (GCP) while redefining what’s possible and revolutionizing the way people interact with technology. Through strict compliance with ethical and regulatory protocols, we focus on ensuring the well-being of our trial participants while advancing the frontiers of neuroscience! Every day will bring fresh challenges and unprecedented opportunities to pioneer new approaches in the pursuit of our mission. From navigating regulatory pathways, designing trial protocols and documentation, and executing clinical trials, our team is instrumental in translating Neuralink’s BCI technology for use in people!

Job Description and Responsibilities:

As a Clinical Scientist I, you will support the development, design, and execution of Neuralink’s clinical evidence strategy. This role focuses on translating product and research objectives into clinical study designs, supporting data analysis, and ensuring scientific rigor across clinical programs.

This individual is  a self-driven and analytically strong individual who can contribute to clinical strategy while executing with precision. The ideal contributor is detail-oriented, collaborative, and comfortable working in a fast-paced, multidisciplinary environment.

In this role, you will:

• Support the design and development of clinical study protocols, including endpoints, inclusion/exclusion criteria, and statistical considerations
• Contribute to clinical strategy by translating research and product goals into evidence-generating study plans
• Partner with other team members to support execution of clinical studies and ensure alignment between scientific intent and operational delivery
• Build and maintain strong working relationships with internal teams, investigators, and external partners
• Support preparation of study-related documents, including protocols, investigator brochures, clinical study reports, and regulatory submissions
• Contribute to EDC and CRF design by ensuring alignment between protocol objectives, endpoints, and data collection strategy
• Translate clinical and scientific requirements into structured, high-quality data capture and validation approaches
• Assist in data review, analysis, and interpretation to evaluate safety and performance outcomes
• Contribute to development of abstracts, presentations, and publications
• Support interactions with ethics committees (e.g., IRB, RECs) and regulatory bodies as needed
• Ensure scientific and clinical activities are conducted in compliance with Good Clinical Practice (GCP), applicable regulations, and internal SOPs
• Identify data trends, inconsistencies, or risks and proactively communicate findings to the broader team

Required Qualifications:

• Familiarity with statistical methods or programming (e.g., Python, R)
• 5+ years of experience in clinical research or scientific roles within medical devices or related fields
• Strong analytical and problem-solving skills with the ability to interpret complex data
• Familiarity with clinical study design, endpoints, and data analysis concepts
• Working knowledge of Good Clinical Practice (GCP) and basic regulatory requirements (e.g., ISO 14155)
• Ability to work cross-functionally with clinicians, engineers, and operational teams
• Strong written and verbal communication skills, particularly in scientific and technical contexts
• High attention to detail and ability to manage multiple priorities

Preferred Qualifications:

• Experience with neurological, neurosurgical, or implantable medical device studies
• Experience supporting protocol development, data analysis, or clinical reporting
• Publications or scientific presentations in biomedical engineering or neuroscience
• PhD  in neuroscience, biomedical engineering, or a related field
  

Additional Requirements and Competencies: 

• Willingness to travel (up to ~20–30%) to support site visits, investigator meetings, and study activities
• Strong organizational and documentation skills
• Ability to work independently while collaborating closely with cross-functional teams
• Adaptability and comfort in a fast-paced, high-growth environment
• Commitment to scientific rigor, patient safety, and high-quality evidence generation

Team Description:

As part of the Surgery & Robot Hardware Department, the Surgical Consumables Team is responsible for producing a wide range of critical mechanical devices that enable our life-changing surgical procedures. Balancing immediate needs with long-term scalability, we drive innovation with precisely engineered tools that ensure safety, reliability, and high-quality surgical execution.

Job Description and Responsibilities:

We’re looking for a Manufacturing Engineer to help scale the manufacturing of consumables used in our robotic surgeries. These consumables include the Needle Cartridge (the end effector that inserts electrodes into the cortex) as well as other complex mechanical assemblies and surgical proxies, like the one being assembled here.

In this role, you will help expand our team’s capabilities by supporting the build-out of a new manufacturing site in Texas while sustaining production at existing sites. You’ll work hands-on to troubleshoot manufacturing issues, analyze data, improve processes, and design fixtures. You will collaborate closely with hardware designers, machinists, quality engineers, and the surgery team to ensure parts are built correctly, released on time, and delivered where they’re needed. 

You will contribute to technical solutions for complex manufacturing problems and help design processes that scale as production ramps. This role is well suited to someone who enjoys working closely with hardware, learning how products move from development to production, and operating in a fast-paced environment. The Manufacturing Engineer will:

• Support day-to-day production to meet consumables demand across the company
• Provide manufacturability input as products move into more mature lifecycle stages
• Design, test, and implement production fixtures, tooling, workstations, and assembly aids
• Troubleshoot manufacturing issues, perform root cause analysis, and implement corrective actions
• Support quality control activities in compliance with Design Control requirements, cGMP, FDA regulations, and internal policies
• Generate and maintain manufacturing documentation, including work instructions, Device Master Records (DMRs), and Design History Files (DHFs)
• Conduct risk assessments and support mitigation efforts to ensure product safety and reliability
• Drive continuous improvement efforts focused on yield, throughput, and process robustness

Required Qualifications:

• Strong interest in manufacturing small, safety-critical assemblies where precision and quality are paramount
• Bachelor’s degree in Mechanical Engineering, Electrical Engineering, Industrial Engineering, Biomedical Engineering, or a related field, or equivalent experience
• 1+ year of experience in manufacturing engineering or engineering design
• Experience in Solidworks (preferred), OnShape, Creo, or an equivalent CAD program
• Demonstrated ability to execute on hardware-focused projects
• Hands-on experience physically building hardware (machining, fabrication, soldering, assembly, prototyping, etc.); personal projects are a plus
• A genuine interest in manufacturing and passion for learning

Preferred Qualifications:

• Experience working in a manufacturing environment
• Familiarity with ISO 13485, FDA 21 CFR Part 820, or other regulated manufacturing standards
  
  

Additional Requirements and Competencies:

• This role will initially require frequent travel to Fremont, CA, which is expected to decrease over time

Senior Platform Engineer

Location: Hybrid

Team: Platform Engineering

Reports to: Senior Director

Type: Full-time

About the Role

We’re building a next-generation Healthcare App Platform — a flexible foundation that enables rapid development of high-quality, customizable healthcare applications. This is not your typical role — we’re building the platform that builds the products.

Healthcare apps share a lot of the same DNA — appointments, care plans, status tracking, forms, communication, reporting. The challenge is in allowing for workflow customization without sacrificing developer productivity or runtime performance.

We’re looking for Senior Engineers to help define and build the service-oriented architecture that powers this platform, in collaboration with in-house SMEs, product, and design partners.

What You’ll Be Doing

• Designing and building core platform services in Node.js / NestJS, focused on performance, modularity, and long-term maintainability
• Modeling complex domains in PostgreSQL, using sound data architecture principles (BCNF/3NF) to power customizable healthcare workflows
• Creating internal tooling, APIs, and libraries that accelerate product teams and enable safe, scalable customization across applications
• Collaborating across product, design, and clinical teams to shape platform capabilities that directly support real-world healthcare use cases
• Enabling front-end teams to build high-quality applications by providing reliable, well-documented service interfaces and reusable UI primitives
• Balancing short-term delivery with long-term vision, making tradeoffs explicit and optimizing for developer velocity, product agility, and platform consistency
• Driving platform adoption by aligning evolution of internal tools with the needs of product and solution delivery teams

What We’re Looking For

• 8+ years of engineering experience, with a strong background in platform or internal tools development
• Deep experience with: 
  • Node.js + NestJS
  • PostgreSQL (including strong data modeling skills)
  • React (used in the context of platform UI libraries and applications)
• Strong cross-functional collaborator: You live and breathe platform engineering, and you evangelize the power of a well-built platform.
• Strong systems thinking: you’ve built frameworks, SDKs, design systems, or internal platforms that scale
• A pragmatic, product-oriented mindset — you’re focused on empowering other engineers through elegant abstractions
• Demonstrated product sense: understands user needs (internal teams), avoids overengineering, and builds with a clear value proposition
• Comfortable building and owning services in a service-oriented architecture
• The strongest candidates have:
  • Experience in healthcare, workflow engines, permissions/RBAC systems, rules engines, or multi-tenant architectures
  • Experience maintaining a fleet of applications built on a common platform
  • Previous Product Management experience
  • Previous consulting or external customer facing experience

Nice to Have

• Experience migrating mission-critical systems onto a new architecture
• Familiarity with Domain Driven Design
• Previous Python development experience

Why Join Us?

• Work on important, meaningful problems in healthcare
• Shape the foundation of a platform that will power dozens (eventually hundreds) of applications
• Collaborate with a team that values design, pragmatism, and velocity
• Competitive compensation, equity, and full benefits

Compensation Disclosure
The anticipated base salary range for this position is $170,000 – $190,000 in the Los Angeles market. Actual offers depend on skills, experience, and location, and may include additional components such as performance bonuses, stock options, and benefits.

Chorus Innovations is proud to be an equal-opportunity employer committed to building a diverse team. We welcome applicants of every background and provide reasonable 
accommodations throughout the hiring process. If you need assistance, email careers@joinchorus.com

POSITION SUMMARY:

The Senior Lab Automation Engineer is an experienced engineer with expertise in the development and implementation of complex laboratory automation and integrated systems. They can work independently to conceptualize, design, develop and implment automated solutions for robust, reliable performance of NGS assays. This development includes standalone instruments and integrated systems. They can work together with cross-fucntional teams of scientists, engineers, and software engineers to deliver these automated platforms. In addition, they can provide high-level support for any of the processes they develop - both at an instrument and an assay results level. This engineer can perform their role independently, but will most often be a part of a larger overall development and will have to be capable of working well in a team environment. They lead by example and contribute to the team beyond their day to day duties.

QUALIFICATIONS:

• Bachelor’s degree in Biomedical Engineering, closely related scientific field or equivalent.
• 4+ years of experience in laboratory automation engineering.
• Technical proficiency and experience in automation and systems development and integration in the life sciences industry; especially with robotics and liquid handling systems.
• Background in NGS laboratories is a plus, as is background in clinical laboratories.
• Experience in software programming and data handling (including database work) is a plus.
• Strong attention to detail and organizational skills required.
• Excellent problem solving skills.
• Strong written and verbal communication skills are required.
• Flexibility to support several simultaneous projects.
• Developing leadership skills. 
• Ability to travel between local Austin sites, within 1 mile, to support multiple labs

KNOWLEDGE, SKILLS, AND ABILITIES:

• Ability to integrate a variety of instruments, such as liquid handlers, plate readers, and plate-handling robotics.

• Software development experience, or minimally familiar with software development practices.

• Excellent communication, organizational, record-keeping, planning, attention to detail and time management skills.

• Comfortable working with a variety of internal teams, and managing relationships with external contractors.

• Experience in programming and operating liquid handlers. (Tecan, Hamilton, etc)

• Experience working with LIMS systems is a plus.

• Strong project management skills, organizational skills, and written and verbal communication skills.

About the Role

The Product Design team is seeking an experienced Senior Product Designer to lead and elevate our design initiatives across a range of applications in the public health sector. We are seeking a designer who is deeply enthusiastic about crafting exceptional user experiences and is dedicated to shaping products that can significantly improve health outcomes for millions. Our leadership team is committed to making a positive impact on the world by bringing top-tier product design expertise to those who need it most: our communities.

The ideal candidate should possess a genuine passion for creating refined user experiences for both native and web applications, catering to both mobile and desktop platforms. Strong collaboration skills are essential, as well as the ability to remain composed in high-pressure situations, adept problem-solving capabilities, meticulous attention to detail, and adaptability in fast-paced environments. Above all, the role requires a dedicated individual who understands Apple-level standards of excellence, and has a design aesthetic that is intentional, simple, and beautiful.

This candidate should be both technical and visionary. They will partner with Technical Platform Product Managers, Data Scientists, and healthcare SMEs to create and evolve the world’s newest, most innovative platform in the healthcare space. The candidate will work on platform product features that span multiple product lines and integrate with complex systems, such as EHRs. The ideal candidate should have experience designing and delivering AI products, while also using AI products in their design and prototyping process.

The candidate will focus primarily on the Chorus platform and its core features, partnering with product line-focused teams to create one unified Chorus product ecosystem.

What You’ll Be Doing

• Lead the end-to-end product design process, from initial concept and user research to wireframing, prototyping, and high-fidelity UI/UX design.
• Collaborate closely with cross-functional teams including product managers, engineers, and healthcare experts to define design objectives and project priorities.
• Develop and maintain design systems, guidelines, and best practices to ensure design consistency and scalability across products.
• Leverage user research and Domain Driven Design (DDD) artifacts, gather insights and design journey maps to inform design decisions.
• Create interactive prototypes to support user testing sessions to validate design concepts and gather user feedback.
• Translate complex user needs and business requirements into simple, intuitive and visually appealing design solutions.
• Mentor and provide guidance to junior designers, fostering a culture of collaboration and design excellence within the team.
• Lead design reviews and provide constructive feedback to peers and team members to continually improve design quality.
• Stay updated with industry trends, emerging technologies, and design methodologies, and share knowledge within the organization (AI, etc).
• Ensure designs are simple, beautiful, and accessible.

What We’re Looking For

• Preferred but not required: Bachelor's degree in Design, HCI, or related field, or equivalent practical experience.
• 5+ years of experience in product design working on technical products, with a strong portfolio demonstrating expertise in UI/UX design for web and mobile applications.
• Experience designing and shipping AI-driven products or features (or experience prototyping AI driven ideas)
• Proficiency in design tools such as Figma (preferred), Sketch, or similar software.
• Extensive knowledge of user-centered design principles, information architecture, and interaction design.
• Proven experience leading design projects and working in Agile development environments.
• Experience in handling several complex projects simultaneously and comfortable with ambiguity and change during a project.
• Strong problem-solving skills and the ability to think creatively to develop innovative design solutions.
• Excellent communication and presentation skills to articulate design decisions and collaborate effectively with cross-functional teams.
• Experience and interest in solving problems that can be highly technical.
• Bonus: Knowledge of healthcare or other highly regulated industries is a plus.
• Bonus: Familiarity with designing platforms or productivity workflow products is a plus.
• Bonus: Domain Driven Design methodology experience is a plus.
• A passion for health equity and our customers is a must

Why You’ll Love Working with Us:

• Engage with an exciting, fast-growing, and diverse group of coworkers dedicated to improving lives by breaking down technology barriers.
• Work in a culturally rich environment that values diversity and inclusivity, ensuring a welcoming and supportive atmosphere for all employees
• Full medical, dental, vision and life insurance benefits
• 401K matching
• Company stock options
• Unlimited paid vacation
• Performance bonuses 
• Company support for career and skill development
• Fun company events and outings
• Chorus is an equal opportunity employer with a commitment to diversity and inclusion

Compensation Disclosure
The anticipated base salary for this position is $141,000 and $161,000 based on the Los Angeles market. The base salary offered may vary depending on several factors, including the applicant's qualifications, relevant experience, specific skills, level of education, certifications, and the geographic location where the role will be performed.

Please note that the listed compensation details apply to the base salary only and do not include additional elements of the total compensation package, such as performance bonuses, stock options, or benefits. The final compensation package will be determined by evaluating the candidate’s qualifications in relation to market standards and internal pay equity.

Head of Sales, US

At Pattern Bioscience, we’re tackling antibiotic resistance, one of the biggest public health challenges of our time.  We use machine learning and microfluidics to quickly identify the bacteria causing an infection and to predict which drugs will cure the infection. Our mission is to reinvent the clinical microbiology lab using our novel, game-changing technology. 

To accomplish our mission, we are seeking an experienced and entrepreneurial Head of Sales - comfortable in the startup, biotech environment to own hospital adoption and revenue growth. The role is ideal for someone who takes pride in building a consistent and effective commercial engine. You will be responsible for direct enterprise selling and building a high-performance team to drive market adoption across hospital systems. This role is for you if you enjoy improving the standard of care in hospitals by selling clinical and economic value. 

How You Will Contribute 

Immediate Priorities: 

• Deliver early revenue traction and adoption in flagship health systems for new product launches 
• Build a process driven Sales team with performance metrics aligned to funnel progression and effective value creation to key stakeholders 
• Demonstrate clear clinical, operational and economic value to hospital stakeholders across lab leadership, pharmacy/antibiotic stewardship, clinicians, value analysis committees and C-suite 
• Navigate and develop strategies to leverage hospital budgeting, IDN and GPO contracting structures 
• Ensure entire team is adequately trained and effective at messaging patient outcome, workflow efficiency, antimicrobial stewardship benefits and cost savings/avoidance value of Pattern’s solutions 
• Recruit, develop and retain top talent aligned with the unique realities of early-stage company and launch of innovative Dx solutions 
• Develop key reference accounts and effectively leverage these to drive sales expansion 

Other Opportunities: 

• Drive multi-site expansion of Pattern’s solutions across IDNs and GPOs 
• Implement CRM discipline, funnel stage action plans and data input accuracy 
• Own key commercial performance metrics to deliver operational excellence in forecasting, sales cycle improvement and Sales Rep productivity 
• Assist with designing territories, compensation structures, and hiring plans aligned to growth milestones and cash efficiency 
• Represent the company with credibility at industry conferences and VIP engagements. 
• Provide structured market feedback to inform pricing, packaging, and product roadmap decisions. 
  
  

 We'd Love to Hear from You If You 

• Foster a culture of disciplined execution, transparency and continuous improvement 
• Commercially driven diagnostics leader who combines clinical credibility, health-system navigation expertise, and value-based selling capabilities with the agility and hands-on execution required to scale an IVD startup 
• Excel in achieving goals and finding creative and effective means to remove obstacles 
• Excel in operating effectively in resource-constrained environments and building processes to maximize team effectiveness 
• Are flexible, adaptable, and comfortable moving through uncertainty to recommend and make decisions 

Desired Education and Experience 

• Bachelor’s degree in Science, Biomedical, Business or related field required. MBA or advanced technical degree (MS, PhD) preferred.  
• Minimum of 12 years of experience in commercial roles in diagnostics, medtech, life sciences required.  
• Proven success launching novel technologies into hospital and fluency in value-based selling. Experience in infectious disease diagnostics is highly preferred. 
• Experience operating in startup or venture-backed environments with limited infrastructure and evolving strategy 
• Strong fluency in healthcare economics, reimbursement pathways, and value-based purchasing. Experience launching products that require behavior change and clinical pathway integration is a plus. 
• Experience in and comfort with pre-revenue startups is a plus. 
  
  

Details  

Location: hybrid in Austin, TX preferred; open to remote with travel 

Type of Position: Full-time 

Join us! We're excited for what you can bring to our team. Here are a few things we provide to make sure you have a great experience. Learn more about our team by visiting our website. 

Benefits 

• Paid Time Off 
• 401K 
• Health Insurance 
• The opportunity to make a global impact 

To fulfill our mission and build world-changing technology, we’ve put together a diverse, multi-disciplinary top-notch team, a culture of innovation, learning, adaptability, and excellence and environment where people love coming to work. 

We value diversity on our teams. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity or expression, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.  

Head of Commercial 

At Pattern Bioscience, we’re tackling antibiotic resistance, one of the biggest public health challenges of our time.  We use machine learning and microfluidics to quickly identify the bacteria causing an infection and to predict which drugs will cure the infection. Our mission is to reinvent the clinical microbiology lab using our novel, game-changing technology. 

To accomplish our mission, we are seeking an experienced and entrepreneurial Head of Commercial comfortable in the startup, biotech environment to own revenue generation, market strategy and growth. The role is ideal for someone who takes pride in driving market adoption of new, innovative diagnostic products. You will be responsible for leading commercial strategy across sales, marketing, market access, clinical value and customer engagement. This role is for you if you enjoy owning the creation of a team and executing at a high-level.  

How You Will Contribute 

Immediate Priorities: 

• Develop and execute the Go-to-Market plan for Pattern’s Pneumonia ID/AST solution 

• Build and manage Sales, Marketing, Customer Service & Support teams and work cross-functionally with all other departments to ensure effective commercial execution 

• Own revenue generation and leverage best-practices in creating and managing performance metrics, funnel development, forecasting and clinical implementation 

• Develop tailored value messaging to key stakeholders in hospitals leveraging workflow, clinical and health-economic value to drive hospital adoption 

• Lead engagement and negotiation with major IDNs and GPOs and C-suite to secure system-wide approval and master agreements 

• Track customer satisfaction, engagement, and product quality and leverage data to drive ongoing product improvement aligned with driving revenue and profitability 

Other Opportunities: 

• Lead pricing, reimbursement, KOL engagement, guidelines and health-economic education to drive customer demand for Pattern’s solutions 

• Own company strategy and product roadmap to drive revenue growth and company value creation 

• Develop and own commercial expansion via alternate channels outside the US 

• Work closely with regulatory and medical affairs on evidence generation tailored to driving revenue growth and market expansion 

• Own the commercial budget and contribute to both annual and long-range revenue and budget planning 

We'd Love to Hear from You If You 

• Commercially driven diagnostics leader who combines clinical credibility, health-system navigation expertise, and value-based selling capabilities with the agility and hands-on execution required to scale an IVD startup 

• Excel in achieving goals and finding creative and effective means to remove obstacles 

• Excel in execution with strong attention to detail while maintaining a strategic, big picture vision 

• Are flexible, adaptable, and comfortable moving through uncertainty to recommend and make decisions 

• Foster strong cross-department relationships and pursue collaborative buy-in 

Desired Education and Experience 

• Bachelor’s degree in Science, Biomedical, Business or related field required. MBA or advanced technical degree (MS, PhD) strongly preferred.  

• Minimum of 15 years of experience in commercial roles in diagnostics, medtech, life sciences required.  

• Demonstrated success building and scaling commercial functions in early-stage or high-growth environment and achieving revenue goals. 

• Experience operating in startup or venture-backed environments with limited infrastructure and evolving strategy 

• Experience in infectious disease diagnostics and launching new, innovative products highly preferred 

• Thorough knowledge of US Hospital Diagnostic Lab customer profile and purchasing process with experience selling to IDNs and working with GPO 

• Experience launching products that require behavior change and clinical pathway integration is a plus 

• Experience in and comfort with pre-revenue startups is a plus 

Details  

Location: onsite Austin, TX preferred; open to hybrid or remote with travel 

Type of Position: Full-time 

Join us! We're excited for what you can bring to our team. Here are a few things we provide to make sure you have a great experience. Learn more about our team by visiting our website. 

Benefits 

• Paid Time Off 

• 401K 

• Health Insurance 

• The opportunity to make a global impact 

To fulfill our mission and build world-changing technology, we’ve put together a diverse, multi-disciplinary top-notch team, a culture of innovation, learning, adaptability, and excellence and environment where people love coming to work. 

We value diversity on our teams. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity or expression, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.  

About the Role

We’re seeking a Senior Data Engineer to help design and build the infrastructure that powers data-driven decision-making and workflow automation across our healthcare platform. You’ll work closely with internal teams, partners, and stakeholders to define and deliver clean, reliable, and scalable data pipelines, with a strong focus on interoperability with EHR systems and healthcare APIs.

This is a high-impact role where you’ll influence architecture, data modeling, integration strategy, and client engagement in a regulated and data-rich environment with a team of engineers dedicated to building the highest quality systems.

What You’ll Be Doing

As a Senior Data Engineer at Chorus, you’ll be flexing your skills across, and providing real impact.

You’ll be:

• Owning and evolving internal data pipelines that support analytics, operations, and end applications
• Enabling self-service analytics and operational insights via semantic layers and tools (e.g. Metabase, Looker, Tableau, Power BI, etc…)
• Designing and maintaining integrations with external healthcare systems (EHRs, FHIR-based APIs, HL7 interfaces, Slack, Google, etc.)
• Collaborating on the development and maintenance of our central Data Warehouse, ensuring clean schema, lineage, and query performance
• Collaborating with product, engineering, and client delivery teams to understand and translate customer domain knowledge into structured data solutions
• Building workflow automation to support care management, reporting, and operational tasks.
• Championing data quality, observability, and governance, especially in regulated healthcare environments in team
• Mentoring engineers and contribute to a culture of knowledge sharing, technical excellence, and continuous improvement

What We’re Looking For

• 8+ years of experience in data engineering or similar roles
• Strong experience with modern data pipeline tools (e.g., Airflow, dbt, dlt, Dagster)
• Proficiency in SQL and Python (or equivalent data engineering languages)
• Experience integrating with EHRs or healthcare APIs (e.g., FHIR, HL7, SMART on FHIR).
• Experience working with HIPAA-compliant data practices, security models, and systems (e.g. encryption, access controls, audit logging, data segregation, data retention, breach detection)
• Experience with data modeling and designing data warehouses (e.g., Snowflake, BigQuery, Redshift, or Postgres-based solutions)
• Strong communication skills with the ability to work with both technical and non-technical stakeholders
• Prior experience in client-facing or consultative roles is a plus

Nice to Have

• Experience with healthcare data standards (LOINC, SNOMED, ICD-10, etc.)
• Exposure to workflow engines, rule engines, or care coordination platforms
• Experience structuring data architecture for MLOps usecases
• Familiarity with infrastructure-as-code and cloud-native tools (e.g., Terraform, AWS/GCP/Azure)
• Familiarity with container orchestration tools (e.g. Kubernetes, OpenShift)
• Background in building data platforms in high-compliance environments

Why You’ll Love Working with Us:

• Engage with an exciting, fast-growing, and diverse group of coworkers dedicated to improving lives by breaking down technology barriers.
• Work in a culturally rich environment that values diversity and inclusivity, ensuring a welcoming and supportive atmosphere for all employees
• Full medical, dental, vision and life insurance benefits
• 401K matching
• Company stock options
• Unlimited paid vacation
• Performance bonuses
• Company support for career and skill development
• Fun company events and outings
• Chorus is an equal opportunity employer with a commitment to diversity and inclusion

Compensation Disclosure
The anticipated base salary for this position is $160,000 to $175,000 based on the Los Angeles market. The base salary offered may vary depending on several factors, including the applicant's qualifications, relevant experience, specific skills, level of education, certifications, and the geographic location where the role will be performed.

Please note that the listed compensation details apply to the base salary only and do not include additional elements of the total compensation package, such as performance bonuses, stock options, or benefits. The final compensation package will be determined by evaluating the candidate’s qualifications in relation to market standards and internal pay equity.