Responsibilities

The Sr Safety Specialist will perform and potentially oversee day-to-day Pharmacovigilance (PV) activities within a highly regulated environment, including collection, monitoring, assessment, evaluation, and tracking of safety information. Responsibilities include working independently on PV activities, participating in on-call duties for specific projects, developing program and departmental procedural documents, conducting audits, mentoring less experienced staff, reviewing regulatory/pharmacovigilance publications, reviewing cases for quality and accuracy, and preparing for and attending client/investigator meetings. The role also involves routine project implementation and coordination, including presentations and review of metrics and budget considerations.