Principal Product Manager, Clinical Trials Intelligence

Opportunity

We are seeking a Principal Product Manager, Clinical Trials Intelligence to build products that help teams plan, run, monitor, analyze, submit, and follow clinical trials with greater speed, quality, and confidence.

This role will define and deliver product strategy across the clinical trial continuum, from study design and startup through trial conduct, submission readiness, and post-approval safety monitoring.

Required Skills, Experience and Education

• 12+ years of experience in Product Management, Clinical Data Product Management, Clinical Informatics, Clinical Operations Technology, Clinical Systems, Digital Health, Life Sciences Data Platforms, or related roles within biotech, pharma, CRO, healthcare technology, or another regulated environment.
• Strong product leadership experience, including defining vision, shaping strategy, building roadmaps, prioritizing tradeoffs, influencing senior stakeholders, and delivering measurable outcomes across complex domains.
• Deep understanding of clinical trial workflows across study design, startup, conduct, monitoring, data management, analysis, submission, and post-approval safety monitoring.
• Experience translating clinical trial workflows into scalable product capabilities, user stories, evaluation criteria, and product requirements.
• Working knowledge of clinical data and systems, including CTMS, EDC, eTMF, IRT/RTSM, eCOA/ePRO, safety systems, clinical data repositories, statistical programming environments, and vendor data feeds.
• Strong understanding of clinical data quality, governance, metadata, lineage, interoperability, access controls, auditability, validation, and regulated system expectations.
• Product judgment to evaluate build, buy, partner, and integration options based on user value, market maturity, compliance needs, scalability, interoperability, and maintainability.
• Strong communication and stakeholder management skills across clinical, regulatory, safety, medical, technical, quality, vendor, and executive audiences.
• Bachelor’s degree or equivalent experience in Life Sciences, Clinical Research, Public Health, Pharmacy, Medicine, Computer Science, Information Systems, Engineering, or a related field.

Preferred Skills

• Experience delivering enterprise clinical data products, clinical intelligence platforms, clinical operations analytics, or AI-enabled clinical decision-support products.
• Experience with oncology clinical development, precision medicine trials, biomarker-driven studies, complex trial designs, or global clinical operations.
• Familiarity with clinical standards and regulatory expectations such as CDISC, SDTM, ADaM, controlled terminology, GxP, 21 CFR Part 11, GDPR, HIPAA, ICH GCP, or related requirements.
• Experience evaluating, implementing, or integrating SaaS platforms and vendor solutions across clinical operations, clinical data management, regulatory, safety, or medical workflows.
• Experience using modern AI, analytics, workflow, and low-code tools to prototype product concepts, validate user needs, and de-risk ideas before full engineering investment.
• Comfort operating in an emerging biotech environment where strategy, execution, ambiguity, compliance, vendor complexity, and hands-on problem solving all matter.