Clinical Development Senior Medical Director, Breast Oncology

Job Summary
Clinical Development Senior Medical Director (individual contributor) for the atirmociclib program.

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 among study teams, investigators, ethics committees, steering committees, and regulatory authorities.
- Lead and contribute to development/maintenance of clinical trial and regulatory documents with Clinical Scientist and cross-functional partners.
- Provide clinical development leadership across multiple study teams; serve as Clinical Development Lead on subteams (including Marketing Authorization Applications).
- Collaborate with Global Development Team to create/refine development strategies.
- Represent the company in external engagements/joint collaborations.
- Collaborate with Clinical Scientists to review/interpret clinical data, identify key findings, and communicate to internal/external stakeholders.
- Maintain clinical expertise by staying current with literature and guidelines.

Basic Qualifications
- Primary medical degree (MD/DO/MBBS/MBChB) and 4+ years biopharmaceutical clinical R&D experience.
- Licensed to prescribe medicines independently for at least 2 years post intern/house officer/foundation.

Preferred Qualifications
- Board certified/eligible in oncology.
- Breast Oncology experience (2+ years).
- Late-phase clinical development experience.

Work Requirements
- Hybrid: commute distance; on-site ~2.5 days/week.
- Travel to scientific conferences/meetings several times per year.
- Relocation support available.