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Job description
Moderna seeks a pharmacovigilance-leaning clinical development professional to support Oncology Therapeutic programs, assisting the Clinical Study Lead in developing, executing, and evaluating Phase 1-3 studies with a focus on data quality for regulatory submissions.
Responsibilities include end-to-end trial delivery, data review, site management, safety collaboration, and authoring core regulatory documents, with in-office 70% at Cambridge, MA or Princeton, NJ and travel up to 15%.
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Worksite address
cambridge, MA, 02140, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.