Pain Clinical Development Director - Hybrid/Remote

Vertex Pharmaceuticals LLC

Boston (MA)

Hybrid

USD 204,000 - 306,000

Full time

8 days ago

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Benefits offered by this job

Annual bonus
Equity awards
Hybrid work design

Job summary

Vertex Pharmaceuticals LLC in Boston, MA is seeking a Clinical Development Associate Medical Director- Pain to lead trial medical strategy and safety oversight. You will serve as the internal Medical Monitor, ensuring scientific integrity of studies and effective collaboration with cross-functional teams on protocol development and regulatory submissions.

Ideal candidates have MD/DO or equivalent, extensive clinical research experience, and familiarity with GCP and regulatory processes.

Qualifications

  • MD/DO or equivalent medical degree with clinical or translational research background.
  • Experience supporting regulatory submissions and study protocols.
  • Familiarity with GCP, study design, and clinical reporting.

Responsibilities

  • Serve as Medical Lead for trials, guiding strategy, design and reporting.
  • Act as internal Medical Monitor, overseeing subject safety and scientific integrity.
  • Participate in protocol development, IBC/IND safety reports and regulatory documents.
  • Collaborate with Regulatory Affairs and Clinical Development teams across Vertex.
  • Represent Vertex in external communications and protocol development.

Skills

Cross-functional leadership
Regulatory interaction
Biostatistics knowledge
Pharmacology & PK
GCP & trial design

Education

MD, DO or equivalent ex-US medical degree

Job description

Vertex Pharmaceuticals LLC in Boston, MA is seeking a Clinical Development Associate Medical Director- Pain to lead trial medical strategy and safety oversight. You will serve as the internal Medical Monitor, ensuring scientific integrity of studies and effective collaboration with cross-functional teams on protocol development and regulatory submissions.

Ideal candidates have MD/DO or equivalent, extensive clinical research experience, and familiarity with GCP and regulatory processes.

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