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Lead complex pharmacovigilance projects and oversee delivery of client services in compliance with regulatory requirements, client specifications, and internal quality standards. Guide and mentor PV teams, coordinate audits and regulatory interactions, and contribute to department strategy, processes, and quality systems.
Purpose of the job position:
· To lead and oversee complex pharmacovigilance (PV) projects, ensuring high-quality service delivery in line with regulatory requirements and client expectations
· To serve as the main point of contact for key PV initiatives and important client projects
· To provide senior-level guidance, mentorship, and supervision to junior PV colleagues and project teams
· To contribute to the development and implementation of department strategy, processes, and quality standards
MAJOR TASKS AND RESPONSIBILITIES:
· Full responsibility for the delivery of complex PV services to clients, including strategic oversight, planning, and coordination of cross-functional PV activities
· Authoring or review of PV documents in compliance with the client´s specification, project-specific instruction, internal working rules, and applicable legislation
· Participation in iVigee quality management system development and maintenance, preparation of internal SOP/working instructions, and preparation of client’s SOPs
· Compliance of PV activities with legislation, internal and client’s procedures
· Participate in or lead interactions with regulatory authorities, including inspections and audit responses; act as audit coordinator during vendor qualification audits, audits conducted as a service for clients, inspections by regulatory authorities, or audits performed by clients on iVigee’s PV services
· Effective deputizing in accordance with the internal responsibility matrix
· Promote knowledge sharing and best practices across PV project teams
· Actively participate in management-level meetings and represent the PV department in cross-functional initiatives
· Maintain current awareness of PV legislation and regulatory guidance and apply it to strategic decision-making
· Mentor, support, and train junior PV team members; provide input into individual development and performance management
· Be open to new areas of vigilance (e.g., medical device vigilance, cosmetovigilance) and participate in building relevant systems
· Support other PV activities as requested
Specific requirements for the position:
Education | University degree in medicine, pharmacology, life sciences or other healthcare professional fields |
Experience | 5+ years of experience directly in pharmacovigilance Pharmacovigilance System Master File (PSMF) authoring and management Local PV Network management Coordination and management of additional Risk Minimisation Measures (aRMM) — an advantage EU QPPV or Deputy EU QPPV role — an advantage |
Special skills | Managerial and organization skills Communication skills Presentation skills Team working Ability to motivate people, leadership |
Language skills | English (fluent) |
Computer skills | Advanced literacy (Microsoft Office applications) |
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