Director, Software Engineering

Department: Product Development

Reports to: SVP, Software Engineering

The Director, Software Engineering is responsible for the delivery of Enterprise SaaS products supporting the Clinical Trial industry, overseeing multiple on-shore and off-shore development teams and the delivery of multiple products and initiatives. The Director, Software Engineering provides strategic planning and tactical execution management, agile release planning across multiple teams, process and tool design, resource management, and continuous improvement. The role demands a blend of technical and business acumen, strategic and tactical focus, and an ability to balance architectural best practice and innovation pragmatism. In a typical business day, the Director, Engineering may find themselves pair-programming with developers on a priority feature or defect and briefing the C-suite on roadmap direction and key technical decisions.  

Responsibilities:

• Works with the SVP of Engineering to build a technical vision for the product line.
• Explores new technologies for future planning and potential implementation and evaluates and identifies appropriate technology to deliver business objectives.  
• Ensures engineering best practices are defined and met across teams and develops and governs technical standards to ensure adherence. 
• Collaborates with architects and principal engineers in the technical design of initiatives and business priorities. 
• Experience leading distributed or cross-functional teams globally, including recruiting, mentoring, and retaining team members in a continuous improvement environment. Provides leadership and professional growth with the goal to build our next generation of engineering leaders. 
• Extensive knowledge of enterprise architecture patterns, microservices, and distributed systems design 
• Experience with enterprise SaaS architecture and development in a product-driven environment, including multi-tenancy, scalability, and platform reliability at scale 
• Fluency in data architecture concepts including data models, data warehouses, analytical platforms, and modern data mesh or lakehouse patterns 
• Familiarity with service portfolio management, API governance, and technical debt prioritization at the enterprise level 
• Works closely with Product Management and Architecture to discover business requirements and technical approach for product initiatives and features. 
• Supports teams in the discovery and design of product backlog items and identifies and manages cross organization dependencies. 
• Develop Proof of Concept solutions to demonstrate technical design and can dive into the code and pair program with engineers as necessary.  
• Initiates and drives continuous improvement initiatives, challenges self and teams to continuously grow and achieve new levels of success. 
• Will be held accountable for the design, development, and delivery of Suvoda product and solutions.  
• A “team-player” with the ability to work within a highly collaborative environment. 
• A creative and critical thinker that is able to confidently express ideas in an articulate, concise manner. 

Requirements:  

• Bachelor’s degree in Computer Science, Information Systems, Mathematics, Engineering or equivalent relevant work experience and/or training. 
• At least 10 years of progressive experience in the software industry, including at least 5 years in a leadership position. 
• Proven experience delivering cloud-native applications on AWS, including IaC tooling (Terraform), container orchestration (EKS), and cloud cost optimization
• Good working knowledge of Python, Django ORM, Django REST Framework, and Angular for building and maintaining scalable backend and frontend services; hands-on familiarity with event-driven cloud service architectures leveraging AWS Lambda, DynamoDB, ElastiCache (Redis), and Postgres RDS 
• Strong experience managing people and teams; setting goals, providing clear technical direction, and holding teams accountable for delivering business value. 
• Strong experience with software development best practices and tooling, agile testing, developer operations, continuous integration and delivery, and site reliability engineering. 
• Relevant technical knowledge of enterprise architecture, cloud services, cloud development, containerization, business domain modelling, data warehouses and analytical platforms. 
• Proven experience in Agile Software Development methodology. 

Nice to Have:

• Hands-on experience adopting and governing AI coding assistants (e.g., Claude, GitHub Copilot, Cursor) across engineering teams, including establishing standards for responsible use, prompt engineering best practices, and measuring productivity impact
• Familiarity with Anthropic's Claude API or Claude Code for agentic developer workflows, including task automation, code generation pipelines, and AI-assisted code review
• Experience integrating LLM-powered tooling into the SDLC — such as AI-assisted test generation, documentation automation, or intelligent PR summarization
• Demonstrated ability to lead organizational change around AI adoption — including upskilling teams, establishing guardrails, and balancing developer autonomy with governance
• Familiarity with prompt engineering principles and the ability to coach engineers on effective human-AI collaboration patterns 

Technical Consultant , eCOA

Reports to: Delivery Lead, Senior Project Manager

Department: Services Delivery  

Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.  

Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda’s software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.  

Responsibilities:

• Primary escalation point for the Suvoda Customer Care team on complex eCOA support issues requiring input from the project team or product development to resolve; troubleshoot escalated issues,identify resolutions , and create Product Support Request when needed.
• Work with assigned clients and project teams responsible for the delivery of eCOA for clinical assessment data collection
• Responsible for overall maintenance of eCOA systems, including oversight of the support process, identification and mitigation of potential issues/risks, and working with the client and other vendors to ensure success using the Suvoda IRT/eCOA system. (inclusive of all modalities)
• Provide direct oversight of other delivery team members as necessary in their performance of related eCOA maintenance duties
• Lead implementation of system change controls for studies during maintenance phase pertaining specifically to eCOA bugfixes. Coordinate with Product Development to advise on the Services needs related to Product updates or fixes.
• Assist with updates to study FAQ documents, used by the customer care team to handle support inquiries and issues, and with maintenance of the FAQ template for eCOA related features/support request.
• Responsible for the system training materials including manuals, walk through videos, and presentations.
• Proactively identify trends in support data and determine the root cause for repeated/frequent support issues; work with the Project Manager, eCOA Practice and other service team members as required to identify and implement solutions
• Identify and assist with the implementation of process improvements for the services department
• Assist the product team with the design and development of new features by providing feedback based on client requests and project experience
• Assist the customer care team with providing support to system users in multiple countries via the telephone and email
• Assist with the training of new staff members on the Suvoda eCOA product and processes
• Perform other related duties as required

Requirements:

• Bachelor's degree or equivalent experience required
• At least 1 year of experience in eCOA/IRT or related field preferred
• Interpersonal and communication skills
• Time management and organizational skills
• Analytical thinking
• Ability to understand technical systems and perform troubleshooting
• Creative problem solving
• Attention to detail

Data Engineer

Department: Product Development 

Reports to: Senior Manager, Data Engineering 

Suvoda is seeking a recent graduate with a passion for data and a strong technical foundation to join our Product Development team. This is an opportunity to launch a data engineering career at Suvoda — a global clinical trial technology company where your work directly helps advance human health. 

As a Data Engineer, you’ll join a collaborative team building a modern, cloud-native data platform. You’ll help build domain-oriented data products using GraphQL APIs and contribute to near real-time reporting through AWS DMS replication to Aurora PostgreSQL.

Responsibilities: 

• Assist in implementing a data mesh architecture using GraphQL APIs to expose domain-owned data products. 
• Help build and maintain an AWS-based data lake using S3, Glue, Lake Formation, Athena, and Redshift. 
• Develop and maintain ETL/ELT pipelines using AWS Glue and PySpark for batch and streaming data workloads. 
• Support AWS DMS pipelines to replicate data into Aurora PostgreSQL for near real-time analytics. 
• Follow best practices for data governance, quality, observability, and API design. 
• Collaborate with product, engineering, and analytics teams to deliver reliable data solutions. 
• Contribute to CI/CD and automation efforts for data infrastructure and pipelines. 
• Stay curious — explore emerging tools and share ideas that could make our platform even better. 

Requirements: 

• Bachelor’s degree in technical fields such as Computer Science or Mathematics. 
• Strong foundational skills in Python and SQL — you’re comfortable writing queries and scripts from scratch. 
• Academic or project experience with data engineering concepts: pipelines, data modeling, or ETL/ELT workflows. 
• Exposure to cloud platforms, particularly AWS (coursework, personal projects, or internships all count). 
• Familiarity with data structures, distributed systems, or database design — you understand the “why” behind the tools. 
• A collaborative mindset and strong communication skills — you ask good questions and explain your thinking clearly. 
• A genuine enthusiasm for data and a desire to keep learning in a fast-moving environment. 

Nice to Have:

• Master’s degree or relevant certifications. 
• Experience with event-driven architectures (e.g., Kafka, Kinesis). 
• Familiarity with data cataloging and metadata management tools. 
• Awareness of data privacy and compliance standards (e.g., GDPR, HIPAA). 
• Exposure to agile development and DevOps practices. 

About Suvoda:
Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease. Headquartered in the greater Philadelphia area, with offices in Bucharest and Iasi, Barcelona, Portland, OR, and Tokyo, JP, we’ve experienced impressive year-over-year growth and are growing our teams across the globe. Learn more about us on our website!

As a Software Developer on Suvoda’s Product team, you’ll design and build clinical trial software that directly supports mission-critical, time-sensitive patient interactions in life-sustaining studies across oncology, CNS, and rare disease. You’ll work in agile, cross-functional teams to deliver high-quality features and services, with a relentless focus on patient safety and the integrity of clinical study data. Here, your code doesn’t just ship product—it helps sponsors, sites, and patients navigate some of the most complex, high-stakes trials in the world, while you grow your craft alongside experienced engineers in a modern, continuously improving SDLC.

Responsibilities: 

• Design, develop, and support clinical trial software with emphasis on patient safety and integrity of clinical study data
• Review product requirements and verify that all requirements can be implemented
• Assist with the creation of technical design and implementation documentation
• Design and code software applications and fix defects
• Provide unit testing coverage for delivered code
• Work with others to ensure timely delivery of high-quality code
• Manage software deployment into all environments and complete all required documentation
• Assist support team with troubleshooting and resolution of production issues
• Perform other related duties as required

Requirements:

• Bachelor’s degree or equivalent experience
• At least 6 years of experience in software development/software engineering
• Deep, hands-on Python experience in production systems
• Deep understanding of relational databases + cloud (AWS) and experience building and supporting services  
• Django experience preferred 
• Angular experience preferred
• Previous exposure to working with AI, with a curious attitude to experiment with Claude Code or something similar 
• Ability to design, develop, and support software modules with medium to high complexity
• Excellent problem-solving skills and learning capability
• Excellent time management and organizational
• Strong production-support mindset for mission-critical payments
  
  #LI-AC1

The Clinical Trial Manager (CTM) is responsible for the oversight and management of all clinical operational activities at the trial and site level. The CTM will interact well with the Heartflow Clinical Research staff and collaborate effectively with Heartflow onsite and field staff, clinical research coordinators, principal investigators, and vendors to aid in ensuring clinical studies meet or exceed timelines and maintain high quality standards. The CTM will have demonstrated experience with clinical research study execution, exceptional organizational skills, excellent attention to detail, and will be comfortable working in a fast- paced start-up culture.

Job Responsibilities:

• Participates in clinical research activities including management of clinical study sites, management of study documentation, vendor management, and completion of project management tasks
• Develops clinical trial timelines, enrollment projections, and instructional materials in support of trial execution, including project, communication, monitoring, recruitment, risk mitigation, and contingency plans
• Participates in and leads process improvement activities within the department and cross functionally, including SOP development
• Conducts study start-up activities including the development of protocols, informed consent forms, source document worksheets, training presentations, etc.
• Reviews site regulatory documents (informed consents, IRB approvals, research agreements) to ensure compliance with study requirements and GCPs
• Maintains effective working relationships with investigators/investigational site research coordinators, and vendors including core labs and data management
• Perform other duties as required for successfully completing studies, as necessary

Skills Needed:

• Ability to work in a smaller team environment with a willing, all hands on deck attitude
• Ability to manage multiple tasks and be comfortable working in an environment with shifting priorities
• High attention to detail, accuracy, and quality and able to effectively prioritize multiple projects
• Knowledge of ICH Guidelines, US FDA, and European clinical trial requirements and regulations
• Excellent written and oral English communication skills required
• Proficiency in computer programs and specifically in Microsoft office tools including Word, Excel and PowerPoint

Educational Requirements & Work Experience:

• Bachelor’s degree in science or health related field
• Demonstrated 5 years minimum relevant experience required
• Experience in cardiovascular medical device clinical research a plus

Travel required: up to 25%

A reasonable estimate of the base salary compensation range is $95,000 to $125,000 and cash bonus. #LI-IB1; 

Suvoda is a global clinical trial technology company shaping digital experiences that enable clinical trial sponsor and site professionals to take full command over the inherent logistical complexity behind mission-critical and time-sensitive patient interactions in life-sustaining studies for therapeutic areas such as oncology, central nervous system, and rare disease.  

Supporting clinical trials means supporting unique experiments that are inherently complex, high-stakes, and dynamic. It is imperative that Suvoda staff working with clients, end-users, or the systems that client and end-users interact with understand the clinical trial industry, regulations, Suvoda’s software products and processes, and especially the specificities of the unique trial in question before taking any actions they may alter the data of the system in question.  

Responsibilities:

• Work within a cross-functional project team to develop Interactive Response Technology (IRT) for randomization and drug supply management
• Review user requirements specifications, verifying that all requirements can be implemented with the Suvodasoftware in the required timeframe 
• Assistwith the creation of implementation design and technical design documentation 
• Develop software systems that are reliable, maintainable, and efficient, with emphasis on patient safety and integrity of clinical study data
• Manage the deployment of SuvodaIRT systems into all environments, completing all required documentation 
• Assistthe support team with troubleshooting and resolution of issues reported on production systems 
• Participate in the product research and development process by providing the engineering team with new solutionsand ideas based on project experience 
• Generate ideas for innovative technological solutions to increase the quality of Suvodasystem 
• Perform other related duties as required
  

Requirements:

• Bachelor’s degree 
• At least 1 year working experience with C#, .NET, and SQL Server
• Familiarity with Web-Services,  ModelView Controller (MVC) and Entity Framework (EF) a plus 
• High achieving personality
• Desire to learn and grow
• Strong work ethic
• Sense of ownership
• Proactive attitude
• Time management and organizational skills
• Attention to detail

#LI-AC1

Haystack Health, a Roivant Health company, is the first clinical trial platform purpose-built for value-based care. We partner with health plans, ACOs, sponsors, and health systems to connect patients to clinical trials that improve outcomes, expand access, and reduce cost.

As a rapidly growing, category-defining company, Haystack operates at the intersection of healthcare delivery, payer strategy, and clinical research. Our model brings together payers, trial sponsors, providers, and research sites to unlock access to clinical trials at scale – fundamentally rethinking how patients are identified, engaged, and enrolled.

About Roivant:

Since its inception in 2014, Roivant Sciences has sought to improve health by rapidly delivering innovative medicines and technologies to patients. We’ve employed a unique, decentralized model of nimble, focused companies (‘Vants’) focused on various therapeutic areas and built around the pursuit of innovation in drug development and technology.

Our model is different. Five new medicines have been approved off the Roivant platform; we’ve built five biotechs that have become public; we’ve created well over $1b in value in Roivant Health in just six years.  Our successes have ranged from computational drug discovery to tokenized healthcare data exchange, and from novel topicals for dermatological conditions to ultrarare tissue therapies.

Roivant Health is Roivant’s platform for the creation of new technology Vants, focused on delivering improvements to human health outside of our traditional biotech platform.  In six years since inception, we’ve created eight enduring companies and over $1B in enterprise value, including the leading deidentified healthcare data exchange platform (Datavant) and a top-tier computational drug discovery company (VantAI) which has partnered with Johnson & Johnson, Bristol-Myers Squibb, and Boehringer Ingelheim. Our goal is to improve human health by rapidly discovering, developing and delivering innovative medicines and technologies to all patients. Our success is predicated on attracting and retaining top talent, generating new ideas and promoting an open and collaborative culture.

Position Location: Remote

Position Summary:

Haystack Health is seeking a Director/VP of Strategy & Operations to lead and scale core operations across our clinical trial programs.

This is a leadership role within a rapidly scaling, high-impact organization. You will own performance across a complex, multi-step clinical operations funnel, driving measurable improvements in patient identification, engagement, and enrollment. You will operate at the intersection of analytics, operations, and execution: diagnosing performance, designing and implementing interventions, and building the systems and teams required to scale.

You will oversee day-to-day operations to understand workflows, identify bottlenecks, and support execution, while also translating these insights into scalable processes, team structures, and operating systems as we grow across clients and geographies.

This is a highly cross-functional leadership role, working closely with clinical, product, and commercial leaders to deliver outcomes for patients and partners, with significant opportunity for growth as the company scales.

Responsibilities:

• Own and improve performance across the end-to-end clinical operations funnel, including patient identification, outreach, engagement, screening, and enrollment, with accountability for measurable outcomes
• Lead structured, data-driven analysis of operational performance to identify root causes of variation, prioritize opportunities, and design and implement high-impact interventions that improve conversion and throughput
• Maintain close proximity to frontline operations to inform strategy, while establishing mechanisms (reporting, QA, performance management) that enable scalable oversight and continuous improvement
• Build and scale operational infrastructure, including workflows, playbooks, training programs, reporting systems, and team structures as the organization grows
• Partner closely with clinical, product, and commercial leaders to translate strategic priorities into operational plans and ensure effective cross-functional execution
• Represent the company as an operational leader in sales processes and partner engagements, helping articulate the model, operational approach, and expected outcomes
• Identify, evaluate, and implement technology and innovative approaches (e.g., AI-enabled outreach, automation, engagement strategies) to improve efficiency, scalability, and outcomes
• Support hiring, onboarding, and management of team members and team leads, and develop capacity models aligned with client growth

Skills, Qualifications, and Requirements:

• Experience in one or more of the following: strategy consulting (healthcare exposure strongly preferred), health tech or tech-enabled services operations, clinical trial operations, or payer/member engagement
• Demonstrated ability to use data and analytics to diagnose operational performance, identify issues, and drive measurable improvements in complex workflows
• Proven experience building, implementing, and scaling operational processes, systems, or teams in dynamic environments
• Experience working cross-functionally with clinical, product, and/or commercial stakeholders, with the ability to translate strategy into execution
• Track record of ownership and accountability for outcomes, with a bias toward action and comfort operating in fast-paced, ambiguous environments
• Strong attention to detail and willingness to operate at both a strategic and highly granular level, including direct engagement with frontline operations
• Demonstrated curiosity, creativity, and openness to testing new approaches, including leveraging technology to improve operational performance
• Exceptional academic background with a bachelor’s degree required; advanced degree (e.g., MBA, MPH, or related field) strongly preferred
• Clinical background is a strong plus, though not required

Roivant Sciences provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws.

We will not accept unsolicited resumes nor outreach from agencies. Please do not send agency resumes to our website or Roivant Sciences and affiliated employees. Thanks!

Job Title: Senior Director, Corporate Operations

Location(s): Pittsburgh, PA or Remote

Job Status: Full-Time

Supervisor: Chief Operations Officer (COO)

Position Overview

The Senior Director, Corporate Operations will report to the COO and play a critical role in driving the execution of Peptilogics’ operational and strategic priorities. This individual will partner with executive leadership to translate business goals into actionable plans, oversee cross-functional operations, and optimize systems and processes to support growth. The Senior Director will have broad exposure across the organization, with a focus on enabling execution, improving scalability, and contributing to key strategic initiatives.

Essential Functions

• Serve as a key operational leader, partnering with the COO and executive team to align strategy with execution
• Lead company-wide operational planning and ensure alignment with strategic goals
• Facilitate forecasts, budget development, resource allocation, vendor payments, and operational performance tracking with Finance
• Implement and improve systems, processes, and tools to drive operational scalability and excellence
• Implement and maintain the Quality Management System (QMS) and oversee SOP creation, updates, and audit readiness
• Ensure compliance across corporate operations, development activities, legal, insurance, and regulatory requirements; foster a culture of compliance
• Oversee management of non-owned physical facilities (labs, offices, external manufacturing sites), IT infrastructure, and enterprise software systems
• Work closely with the Development team to manage relationships with CROs, CMOs, and preclinical and clinical trial providers
• Lead sourcing, procurement, and logistics to support research, development, and external manufacturing operations
• Negotiate contracts and ensure cost-effective resource utilization across all operational activities
• Manage HCP contracting and compliance processes
• Serve as primary point of contact for legal service vendors and coordinate legal operational needs
• Identify operational risks, gaps, and bottlenecks, and proactively lead solutions
• Manage the Operations team including hiring, performance, coaching, and career development
• Drive operational KPIs and reporting, including preparation of materials for executive and board updates
• Ensure operational compliance with company policies, regulatory requirements, and best practices

Additional Duties and Responsibilities

• Support business development and partnership activities through operational due diligence and integration planning
• Support fundraising and investor relations by providing operational insights, data, and reporting
• Support cross-functional teams (R&D, Commercial, Project Management) in executing strategic initiatives
• Collaborate with the COO and Finance on long-range planning and scenario modeling
• Contribute to shaping company culture by supporting initiatives around collaboration, communication, and team building
• Perform other duties as assigned

Required Qualifications and Skills

• Bachelor’s degree in a relevant field (e.g., life sciences, business, engineering); advanced degree (MBA, MS, PhD) preferred
• 10+ years of experience in biotech, pharmaceutical, or life sciences operations
• 3–5 years in a leadership or senior operations role, ideally in a high-growth or venture-backed environment
• Experience scaling operations in a startup or growth-stage company (preferred)
• Prior operational involvement in fundraising, investor relations, or board reporting (preferred)
• Strong project management and organizational skills, with the ability to manage complex, cross-functional initiatives
• Excellent financial and business acumen; experience with budgets, forecasts, and KPIs
• Proven ability to build, lead, and develop teams
• Deep understanding of operational compliance, including legal, regulatory, quality management (QMS), and audit readiness
• Proven ability to build, lead, and develop teams across diverse operational functions
• Exceptional interpersonal and collaboration skills, with the ability to influence at all levels
• Outstanding verbal and written communication skills, including executive-level reporting and presentations
• Excellent verbal and written communication skills, including executive-level reporting and presentations
• Ability to thrive in a dynamic, fast-paced environment with shifting priorities
• Ability to drive cross-functional alignment and collaboration across scientific, operational, and corporate teams
• Strategic thinking and ability to scale operations in a growth-stage environment or commercialization-ready biotech environment
• Experience with contract development, procurement, and resource optimization
• Familiarity with QMS implementation, SOP development, and compliance frameworks in a biotech/pharma setting
• Financial fluency to support investor relations, board reporting, and fundraising activities
• Familiarity with technology-driven R&D environments including computational biology, machine learning
• Change management and process improvement capabilities
• Experience managing HCP engagement processes and ensuring compliance in clinical development