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Integrated Resources INC

Clinical Trials Safety Data Manager

MA · 132 months ago

Full-time

About the job

Job Description Client: Direct Client Location: Cambridge, MA Job Title: Safety Data Collection Manager Duration: 1 year Responsibilities • Responsible for managing the Pharmacovigilance (PV) operations of Pre and Post-approval Clinical Studies globally. • Supports the Senior Manager, Safety Data Collection Clinical Trials and is responsible for setting the safety operations strategy, establishing the safety report collection standards and processes, and ensuring they are implemented and executed consistently throughout all Pre and Post-Marketing Clinical Studies globally. • Clinical Trials Associate will provide partner / vendor oversight in relation to Clinical Trial safety report...