Vice President, Clinical Development, Evidence, and Strategy
New
United StatesFull-TimeVp
Salary266,000 - 346,000 USD per year
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Job Details
- Experience
- 12+ years of leadership experience in clinical research and scientific functions
- Required Skills
- Artificial Intelligence
Requirements
- M.D. or equivalent advanced degree in medicine.
- 12+ years of leadership experience in clinical research within academic, health system, or medical device/pharma industries.
- Track record of leading pivotal FDA studies (IDE, PMA, or NDA/BLA) from design through approval.
- Experience as a Principal Investigator for user experience, design validation, premarket, and post-market studies.
- Expertise in clinical trial design, sample size estimation, and statistical methodology for Class II diagnostic devices.
- Experience managing multidisciplinary teams and scaling organizations.
- Demonstrated success translating clinical evidence into regulatory approvals and commercial adoption.
- Strong communication and executive leadership skills.
Responsibilities
- Lead the company’s overarching clinical strategy and evidence roadmap.
- Define and validate clinical use cases based on unmet needs and technical feasibility.
- Execute pivotal FDA and global regulatory studies with methodological rigor.
- Integrate real-world evidence into regulatory submissions and payer dossiers.
- Own the strategic development of the Research as a Service (RaaS) program.
- Lead multidisciplinary teams including biostatistics, clinical data, and research operations.
- Partner with Product, Regulatory, and R&D teams to align clinical pathways with business goals.
- Represent the organization to regulatory agencies, professional societies, and academic partners.
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