Job Summary
The Senior Medical Director provides clinical development expertise for late-stage thoracic oncology clinical trials, overseeing design, conduct, and analysis, and may supervise other medical directors. Works with regulatory affairs, pharmacovigilance, biostatistics, and medical affairs; provides guidance to clinical operations, investigators, and external stakeholders.
Responsibilities
- Conduct medical monitoring: eligibility assessment, data review, safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as point of contact for clinical issues between study team, investigators, ethics/steering committees, and regulatory authorities.
- Lead and maintain clinical trial and regulatory documents with Clinical Scientist and cross-functional team.
- Execute clinical development strategies as part of the Clinical Subteam (Global Product Team).
- Represent the company in external engagements (advisory boards, health authority interactions).
- Review/interpret clinical data, identify key findings/implications, and communicate to stakeholders.
- Stay current on literature and guidelines to advise and drive development plans.
Qualifications/Required
- Medical degree required.
- 5+ years industry experience required.
- Clinical Development experience required.
- Primary medical degree (MD/DO/MBBS/MBChB) from a recognized institution.
- Licensed to prescribe medicines independently for at least 2 years after intern/house officer/foundation period.
Preferred
- Late-stage clinical development; Thoracic Oncology.
- Board certified/eligible in oncology.
- Maintained medical license in good standing.
Work & Compensation
- Hybrid: live within commuting distance; ~2.5 on-site days/week.
- Travel to meetings several times/year.
- Relocation assistance may be provided.
- Base salary: $274,500β$457,500; bonus target 25%; eligible for share-based incentives; comprehensive benefits include 401(k) with company match, paid leave, and medical/dental/vision.