VP, Clinical Development (CNS & Rare Diseases)

Hw3 Llc

United States

On-site

USD 250,000 - 500,000

Full time

42 hours ago
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Job summary

Compassionate leadership and a strong medical background are essential for the Vice President, Clinical Development role in a small biotech setting. The candidate will guide clinical strategy and oversee execution across programs from early development through pivotal trials and regulatory submissions.

We seek an MD with deep biotech/pharma experience, preferably with neuroscience or rare disease exposure, and a proven track record in leading cross-functional teams, trial design, and regulatory

Qualifications

  • MD required with biotech/pharma development experience.
  • Experience in neuroscience, CNS, and/or rare disease indications preferred.
  • Proven lead of clinical development programs from early stage through Phase 2/3 and pivotal trials.
  • Strong in designing clinical trials, development plans, and regulatory strategy.
  • Experience contributing to IND, NDA, BLA, and/or MAA submissions and regulatory interactions.
  • Strong medical oversight including medical monitoring, data review, and safety/efficacy interpretation.
  • Demonstrated leadership, managing cross-functional teams and external partners.
  • Ability to balance strategic leadership with hands-on involvement in a small biotech environment.

Responsibilities

  • Provide strategic and medical leadership across clinical development programs.
  • Oversee clinical strategy and execution from early development through pivotal trials and regulatory submissions.

Skills

Clinical development
Regulatory strategy
Trial design
IND/NDA submissions
Medical oversight
Cross-functional leadership

Education

MD degree

Job description

Compassionate leadership and a strong medical background are essential for the Vice President, Clinical Development role in a small biotech setting. The candidate will guide clinical strategy and oversee execution across programs from early development through pivotal trials and regulatory submissions.

We seek an MD with deep biotech/pharma experience, preferably with neuroscience or rare disease exposure, and a proven track record in leading cross-functional teams, trial design, and regulatory

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