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Grifols, S.A. is seeking a Pharmacovigilance Specialist to provide operational support for global pharmacovigilance activities and ensure timely regulatory reporting. The role includes data review, analysis, and management of the integrated safety database.
Responsibilities include processing adverse event case reports, performing follow-up, notifying regulators, drafting PSURs, and contributing to SOPs and training. Travel within the United States may be required as part of CAPA and audits.
Grifols, S.A. is seeking a Pharmacovigilance Specialist to provide operational support for global pharmacovigilance activities and ensure timely regulatory reporting. The role includes data review, analysis, and management of the integrated safety database.
Responsibilities include processing adverse event case reports, performing follow-up, notifying regulators, drafting PSURs, and contributing to SOPs and training. Travel within the United States may be required as part of CAPA and audits.