Senior Medical Director, Clinical Development & Strategy

Vertex Pharmaceuticals

Boston (MA)

Hybrid

USD 320,000 - 480,000

Full time

14 days+
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Benefits offered by this job

Medical, dental and vision benefits
Generous paid time off
Educational assistance programs
Generous commuting subsidy
Matching charitable donations
401(k)

Job summary

Vertex Pharmaceuticals is seeking an Executive Medical Director, Clinical Development to shape and lead clinical development strategies for povetacicept renal programs. You will collaborate with Medical Affairs, Regulatory, R&D, and Commercial leaders to drive innovative approaches and ensure program success across global teams.

The role requires MD/DO with extensive pharmaceutical development experience, strong leadership, and a track record of interacting with regulators.

Qualifications

  • MD, DO or equivalent ex-US medical degree.
  • 15 years pharmaceutical industry experience including time managing clinical trials or development programs.
  • 7 years of management experience.
  • Experience interacting with regulatory authorities is highly desired.
  • Ability to work in a fast-paced, matrix environment with strong leadership.

Responsibilities

  • Provide clinical development recommendations to project teams, optimizing study design and conduct.
  • Plan worldwide clinical development activities and guide multidisciplinary teams.
  • Review study protocols and Investigator Brochures; oversee medical monitoring of trials.
  • Interface with regulatory authorities to support development objectives.
  • Ensure compliance with regulatory requirements and Vertex SOPs.

Skills

Global clinical research experience
Regulatory affairs experience
Leadership abilities
Excellent communication skills
Matrix environment collaboration

Education

MD/DO or equivalent ex-US medical degree

Job description

Vertex Pharmaceuticals is seeking an Executive Medical Director, Clinical Development to shape and lead clinical development strategies for povetacicept renal programs. You will collaborate with Medical Affairs, Regulatory, R&D, and Commercial leaders to drive innovative approaches and ensure program success across global teams.

The role requires MD/DO with extensive pharmaceutical development experience, strong leadership, and a track record of interacting with regulators.

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