Clinical Development Medical Director, Oncology

Job Responsibilities
- Collaborate with Clinical Scientist(s) to provide clinical leadership across 2-3 study team(s) that is scientifically rigorous and aligns with company objectives.
- Conduct medical monitoring activities including eligibility assessment, data review, and safety monitoring.
- Lead peer-to-peer interactions with investigators.
- Serve as the point of contact for clinical issues between the 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 team).

Strategic Guidance, Clinical Insights & Interpretation
- Collaborate with Clinical Scientist to review and interpret clinical data, identify key findings and implications, and communicate to internal and external stakeholders.
- Stay abreast of latest developments, literature, and guidelines to advise on and drive current and future clinical development plans.

Basic Qualifications
- Medical degree (Required)
- Clinical Development experience (required)
- 2-5 years industry experience (required)

Preferred Qualifications
- Late-stage clinical development experience
- Thoracic experience
- Board certified/eligible in oncology or equivalent

Benefits
- Eligible for Global Performance Plan with 25.0% bonus target and share-based long-term incentive program
- 401(k) with company matching contributions; additional retirement savings contribution
- Paid vacation/holidays/personal days; paid caregiver/parental and medical leave
- Health benefits (medical, prescription drug, dental, vision)

Work/Travel
- Ability to travel to conferences and team meetings (~4 times/year)
- Hybrid role: live within commuting distance; work on-site ~2.5 days/week

Organizational Relationships
- Reports to Global Development Lead or Senior/Executive Medical Director

Relocation
- Relocation assistance may be available