Clinical Development Senior Medical Director, Oncology

Job Responsibilities

• Provide clinical development expertise for late-stage thoracic oncology clinical trials, including oversight of study design, conduct, and analysis; may supervise (associate) medical directors.
• Conduct medical monitoring: eligibility assessment, data review, and safety monitoring.
• Lead peer-to-peer interactions with investigators.
• Serve as point of contact for clinical issues among study team, investigators, ethics committees, steering committees, and regulatory authorities.
• Lead and contribute to development and maintenance of clinical trial and regulatory documents with Clinical Scientist and cross-functional teams.
• Execute clinical development strategies as part of the Clinical Subteam of the Global Product Team (GPT).
• Represent the company in external engagements (advisory boards, health authority interactions).
• Review and interpret clinical data; communicate key findings and implications to internal/external stakeholders.
• Maintain up-to-date clinical expertise to advise and drive current/future clinical development plans.

• Medical degree required.
• 5+ years industry experience required.
• Clinical Development experience required.
• Primary medical degree (MD/DO/MBBS/MBChB) from a recognized school/university.
• Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation period.

• Late-stage clinical development;
  Thoracic Oncology experience.
• Board certified/eligible in oncology or equivalent.
• Maintained medical license/registration in good standing.

• Hybrid role; live within commuting distance; work on-site ~2.5 days/week. Travel to meetings/conferences several times/year. Relocation assistance may be provided.

• Bonus target: 25% of base salary; participation in share-based long-term incentive. Health benefits and paid time off (401(k) with company matching and additional retirement contribution).