Collaborate with medical, ops strategy, and BD leaders to support client engagement.
Support BD and Proposals in RFPs; prepare medical sections; assist bid defenses.
Write/edit scientific content of deliverables within budget and timelines.
Collaborate with Regulatory Affairs on regulatory strategy as part of drug development.
Review labs, AEs, coded data, and data listings; serve as medical resource.
Own medical and safety monitoring on assigned projects.

🎯 Requirements

MD, DO, MBBS, or equivalent.
5+ years oncology clinical experience.
Ability to analytically assess oncology trial protocols.
Willingness to travel domestically and internationally (≈30%).

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