Related skills
regulatory affairs clinical research medical writing oncology study designπ Description
- Collaborate with Medical, Strategy, and BD leaders to support client engagements.
- Support BD/Proposals in RFPs; draft medical sections and assist bid defenses.
- Write or edit scientific content within budgets and timelines.
- Collaborate with Regulatory Affairs on product landscape and strategy.
- Provide scientific insights for company releases (white papers, manuscripts).
- Review protocols, CRFs, training materials, and study designs.
π― Requirements
- MD, DO, MBBS or equivalent.
- 5+ years of clinical experience.
- Completed an accredited medical residency program.
- Completed oncology/hematology fellowship or equivalent.
- 5+ years in oncology or autoimmune disease clinical research.
- Availability for domestic and international travel (~30%).
π Benefits
- Discretionary annual bonus
- Health insurance
- Retirement savings benefits
- Life insurance
- Disability benefits
- Parental leave
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