Clinical Development Medical Director, Endocrinology (Hybrid)

Physician Pivot

Boston (MA)

Hybride

USD 240 000 - 360 000

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Résumé du poste

Vertex is seeking a Clinical Development Medical Director to serve as Medical Lead for multiple trials across all phases, collaborating with cross‑functional teams to shape strategy, design, and execution. This role drives scientific input, safety monitoring, and regulatory alignment within Vertex clinical programs.

The ideal candidate holds an MD/DO, 10+ years in research, board eligibility, and strong knowledge of trial design, GCP, and biostatistics.

Qualifications

  • MD/DO or equivalent medical degree required.
  • Board certification/eligibility highly desired.
  • Typically requires 10 years of basic or clinical research experience.
  • Working knowledge of biostatistics, GCP, and clinical study design.

Responsabilités

  • Lead development of study protocols, Investigator Brochures, and clinical development plans with cross‑functional teams.
  • Serve on cross‑functional Study Execution Teams (SET) for assigned trials.
  • Prepare regulatory submissions and safety reports for regulatory authorities and ethics committees.
  • Provide scientific input to ICFs, CRFs, SAPs, CPAPs, and CSR; liaise with Translational Medicine/Clinical Development.
  • Represent Vertex to external medical personnel in protocol development and study conduct.
  • Perform other duties as assigned related to clinical programs.

Connaissances

Oral and written communication
Cross-functional teamwork
Biostatistics knowledge
GCP knowledge

Formation

MD/DO or equivalent ex-US medical degree
Board certification/eligibility
10+ years of clinical research experience
Clinical trial design knowledge

Description du poste

Vertex is seeking a Clinical Development Medical Director to serve as Medical Lead for multiple trials across all phases, collaborating with cross‑functional teams to shape strategy, design, and execution. This role drives scientific input, safety monitoring, and regulatory alignment within Vertex clinical programs.

The ideal candidate holds an MD/DO, 10+ years in research, board eligibility, and strong knowledge of trial design, GCP, and biostatistics.

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