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Key Responsibilities:
- With guidance from the Associate Director, ClinOps, responsibility for day-to-day activities within a region or regions, including site selection, start-up, maintenance, and close-out activities.
- May serve as the key operational contact for Braveheart Bio studies aiding in site selection, study implementation, and ongoing coordination of study sites, either directly or via CROs.
- Assist Associate Director, ClinOps with oversight of CRO and set-up of vendors as required, including liaising with Global CRO to ensure timely initiation of study.
Required Experience & Skills:
- At least 4+ years of relevant experience with a BS or BA in a relevant scientific discipline or an RN.
- Relevant clinical trial experience in the pharmaceutical or biotechnology industry.
- Experience as the regional lead for Europe, United States, Latin America, and/or APAC.
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 rapidly evolving therapeutic area.