The Pharmacovigilance Scientist serves an integral role in safety data analyses for assigned investigational and/or marketed product(s) in partnership with the Safety Physician. The Pharmacovigilance Scientist is expected to be equally effective working collaboratively and independently. She/he will support activities such as signal management, aggregate reports, RMP development, ad hoc safety query responses, and literature surveillance.
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USD/year
Spearhead clinical trial activities and support the continued growth of our clinical operations function here at Entrada. Lead in the day-to-day operations, planning, set-up, execution, and closeout of assigned clinical trials. Support and oversee the planning and management of the operational aspects, including CRO and vendor oversight, to achieve project milestones and clinical study timelines.