Oncology Clinical Development: Associate Medical Director

C4-Therapeutics-Inc

Watertown (MA)

On-site

USD 231,000 - 255,000

Full time

14 days+
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Job summary

C4 Therapeutics, a clinical-stage biopharmaceutical company, is seeking an Associate Medical Director to guide and support clinical programs, collaborate with cross-functional teams, and partner with Program Teams across R&D to map regulatory pathways. The role emphasizes advancing science and improving patient outcomes in cancer therapies.

The candidate will work with Health Authorities, investigators, and trial sites to ensure high-quality data and timely regulatory submissions, while

Qualifications

  • MD or international equivalent with at least one year of clinical research in pharma, CRO, or academia.
  • Ability to balance strategic vision with hands-on execution in a fast-paced matrix environment.
  • Excellent scientific communication and stakeholder engagement.
  • Strong interpersonal, negotiating, and problem-solving skills.
  • Strong analytical and attention to detail.

Responsibilities

  • Drive development programs across oncology with cross-functional teams.
  • Provide medical oversight for assigned trials and safety.
  • Engage with investigators, health authorities, and key opinion leaders.
  • Prepare regulatory input for filings with Senior Medical Director.
  • Collaborate globally on regulatory submissions and trial design.

Skills

MD degree
Clinical research experience
Scientific communication
Interpersonal skills
Analytical skills

Education

MD or international equivalent

Job description

C4 Therapeutics, a clinical-stage biopharmaceutical company, is seeking an Associate Medical Director to guide and support clinical programs, collaborate with cross-functional teams, and partner with Program Teams across R&D to map regulatory pathways. The role emphasizes advancing science and improving patient outcomes in cancer therapies.

The candidate will work with Health Authorities, investigators, and trial sites to ensure high-quality data and timely regulatory submissions, while

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