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Key responsibilities:
- Lead the end-to-end clinical data management strategy for Phase 3 and late-stage clinical trials
- Serve as the primary data management point of contact for internal cross-functional teams.
- Ensure CRO-executed data management activities support reliable interim reviews.
Required experience & skills:
- At least 8 years of progressive experience in clinical data management within the biotechnology or pharmaceutical industry.
- Strong CRO and vendor oversight experience, with a track record of driving accountability and quality.
- Demonstrated ability to work cross-functionally in a lean, fast-paced development environment.
Preferred experience & skills:
- Advanced degree in a scientific or quantitative discipline
- Experience in cardiovascular and/or rare disease clinical development
- Prior experience in a small or mid-sized biotech environment transitioning into late-stage development
Braveheart Bio
Braveheart Bio is a Bay Area–based biopharmaceutical company pioneering best-in-class therapies for cardiovascular disease. With a proven leadership team, a strong financial foundation, and a high-value late-stage asset, Braveheart Bio represents an outstanding opportunity for ambitious, mission-driven professionals to make a tangible impact in a high-profile and rapidly evolving therapeutic area.