Clinical Development Medical Director — Hybrid/Remote

Vertex Pharmaceuticals Inc (US)

Boston (MA)

Hybrid

USD 204,000 - 306,000

Full time

3 days ago
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Benefits offered by this job

Hybrid-Eligible
On-Site Eligible

Job summary

Vertex Pharmaceuticals, Inc. is seeking a Clinical Development Associate Medical Director to serve as Medical Lead for clinical trials, overseeing safety and scientific integrity. You will monitor trials, collaborate with cross-functional teams, and contribute to regulatory submissions and publications.

The role supports a hybrid work model with on-site and remote flexibility. Ideal candidates have MD/DO training, 8+ years in clinical research, and experience interacting with regulatory

Qualifications

  • MD/DO or equivalent medical degree required.
  • Strong written and oral communication skills.
  • Experience in global clinical research and regulatory interactions a plus.
  • Familiarity with biostatistics, pharmacology, PK/PD and ICH-GCP standards.
  • Board certification/eligibility in a relevant medical specialty is highly desired.

Responsibilities

  • Lead medical monitoring and trial oversight across studies.
  • Participate in protocol development, regulatory documents, and data analysis plans.
  • Collaborate with cross-functional teams to ensure scientific integrity and compliance.
  • Represent Vertex with external medical personnel and regulatory bodies.

Skills

Communication skills
Collaboration
Global clinical research
GCP & study design
Board certification/medical specialty

Education

MD/DO or equivalent

Job description

Vertex Pharmaceuticals, Inc. is seeking a Clinical Development Associate Medical Director to serve as Medical Lead for clinical trials, overseeing safety and scientific integrity. You will monitor trials, collaborate with cross-functional teams, and contribute to regulatory submissions and publications.

The role supports a hybrid work model with on-site and remote flexibility. Ideal candidates have MD/DO training, 8+ years in clinical research, and experience interacting with regulatory

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