Remote Medical Director, Oncology Clinical Development

Relay Therapeutics; Cambridge (MA); Remote; USD 213,000 - 304,000; Full time

Job summary

Relay Therapeutics in Cambridge, MA seeks a Medical Director to lead clinical strategy from IND to proof-of-concept and registration. You will collaborate with senior medical staff to drive trial design and execution, working cross-functionally with regulatory, biostatistics, and medical writing teams.

A dynamic, fast-paced environment demands strong communication, leadership, and oncology expertise. You will oversee safety and pharmacovigilance, support site initiation, and translate new

Qualifications

• Team player with strong communication skills.
• Experience in oncology and solid tumor programs.
• 5+ years in clinical development in academia or industry.
• Exposure to trial design, protocol development and analysis plans.
• Proven ability to interact with investigators and regulatory bodies.

Responsibilities

• Collaborate with senior medical staff to design and execute early clinical development plans.
• Write clinical sections of Investigator’s Brochures, IND summaries, CTAs and respond to questions from authorities.
• Provide medical review and interpretation of clinical data for leadership and stakeholders.
• Manage drug safety and pharmacovigilance activities for trials.
• Integrate new clinical insights into development plans and trial activities.
• Collaborate with research and drug discovery to shape the portfolio.
• Ensure compliance and ethics in trial design, conduct and reporting.

Skills

Team player

Communicator

Solid tumors

Clinical development

Regulatory collaboration

Education

MD/PhD or equivalent

Job description

Relay Therapeutics in Cambridge, MA seeks a Medical Director to lead clinical strategy from IND to proof-of-concept and registration. You will collaborate with senior medical staff to drive trial design and execution, working cross-functionally with regulatory, biostatistics, and medical writing teams.

A dynamic, fast-paced environment demands strong communication, leadership, and oncology expertise. You will oversee safety and pharmacovigilance, support site initiation, and translate new