A company is looking for a PV Scientist.
Key Responsibilities :
Lead / support safety signal management (detection, evaluation, reporting)
Manage aggregate reports (PSURs, DSURs, RMPs, REMS)
Oversee safety activities for clinical trials
Required Qualifications :
Minimum 7 years of Pharmacovigilance experience, including aggregate safety reports and safety signal management
Bachelor's Degree in biologic or natural science or health care discipline required; advanced degree preferred
Knowledge of MedDRA terminology and its application
Pharmacovigilance Scientist • Lincoln, Nebraska, United States
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