Associate Director, Clinical Science
Bristol Myers Squibb · Rayzebio +1 more
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Role summary
This Associate Director position supports clinical development of radiopharmaceutical oncology therapies at RayzeBio, a Bristol Myers Squibb subsidiary. Responsibilities include protocol development, clinical trial oversight, data management, regulatory documentation, and cross-functional collaboration. The role requires an advanced degree with 6+ years of drug development experience, or a bachelor's degree with 8+ years of relevant background.
What they're looking for
- Master's degree with 6+ years drug development experience, or Bachelor's in biological sciences with 8+ years
- Minimum 5 years clinical research or clinical pharmacology experience in biotech/pharma or CRO
- Knowledge of FDA, EMA, and ICH regulations and guidelines
- Proficiency with Microsoft Office and analytical software like Spotfire
- Strong cross-functional collaboration and interpersonal skills
- Ability to quickly learn new therapeutic areas and adapt to changing priorities
- PharmD or PhD preferred
What you'll be doing
- Develop study concept synopses, protocols, and study design documents with appropriate oversight
- Contribute to clinical data review, analysis, and reporting throughout ongoing trial programs
- Organize and prepare materials for Data Review Committee meetings and investigator communications
- Assist in preparation and review of regulatory documents including INDs, Investigator Brochures, and NDA/MAA filings
- Address scientific questions from investigators and support clinical study implementation and closeout activities
Privacy & handoff
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