What You Will Achieve
- Clinical Development Leadership on Study Teams and Development Subteams
- Serve as the Clinical Development Lead on subteams, including for Marketing Authorization Applications.
- Conduct medical monitoring activities (eligibility assessment, data review, safety monitoring).
- Lead peer-to-peer interactions with investigators.
- Serve as point of contact for clinical issues between study team and investigators.
- Lead and contribute to development and maintenance of clinical trial and regulatory documents with the Clinical Scientist and cross-functional team.
- Strategic Guidance, Clinical Insights & Interpretation
- Collaborate with the Global Development Team to create and refine development strategies.
- Represent the company in external engagements and/or committee participation in joint collaborations.
- Support regulatory interactions.
- Collaborate with Clinical Scientist to review/interpret clinical data, identify key findings and implications, and communicate to internal/external stakeholders.
- Stay current on developments, literature, and guidelines to advise on and drive clinical development plans.
What You Will Need (Basic Qualifications)
- Medical degree with 5+ years clinical/industry experience.
- Hematology/Oncology clinical experience (academia/industry).
- Late-stage clinical development experience.
- Experience providing clinical development leadership across several study teams.
- Excellent communication skills to present complex technical concepts.
- Strong strategic and analytical skills.
Bonus To Have (Preferred Qualifications)
- Leadership or management experience.
- Board certified/eligible in hematology/oncology (preferred).
- Experience across multiple phases of clinical development and across oncology drug classes.
- Late clinical development experience in hematology (highly preferred).
Work Location Assignment
- Hybrid role; live within commuting distance and work on-site ~2.5 days per week.