Drug Safety Specialist
Virtual Vocations Inc
Leading the development and maintenance of Pharmacovigilance Risk Management Plans (PV-RMPs), the full-time Pharmacovigilance Risk Management Specialist will ensure compliance with regulatory requirements while collaborating with cross-functional teams to support patient safety initiatives in a remote work environment. Key responsibilities Serve as the primary author of PV-RMPs, ensuring adherence to global regulatory standards Coordinate cross-functional review and approval processes for PV-RMPs and respond to regulatory authority inquiries Manage project timelines and deliverables related to risk management plans independently Required qualifications Bachelor's degree in Nursing, Biological Sciences, Medical, Clinical, or a related field Minimum two years of pharmaceutical industry experience in Pharmacovigilance or related functions Two to three years of experience authoring Pharmacovigilance Risk Management Plans (PV-RMPs) Knowledge of global PV-RMP regulations and regulatory submission requirements Experience interacting with regulatory authorities and addressing health authority inquiries Virtual Vocations Inc
Vacancy posted 2 days ago
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