Local Safety Officer Coordinator
Il y a 4 semaines
, Casablanca-Settat, Maroc
ProductLife Group
Temps plein
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Gratuit avec email ou Google
At ProductLife Group (PLG), we support life sciences companies throughout the entire product lifecycle, combining local expertise with global reach. As part of our continued growth, we are looking for a Local Safety Officer Coordinator to join our Safety & Vigilance team.
Your Mission
As a Local Safety Officer Coordinator, you will be responsible for the setup, coordination, and oversight of local pharmacovigilance activities across multiple countries, ensuring compliance with local regulations, client requirements, and internal quality standards.
Key Responsibilities
Coordinate and oversee local pharmacovigilance activities for assigned safety projects. Ensure compliance with local and global PV regulations and timelines. Act as the primary operational contact for clients. Manage project tracking, reporting, and activity planning. Prepare, review, and maintain Pharmacovigilance Agreements (PVA), Safety Data Exchange Agreements (SDEA), and Technical Agreements. Monitor project quality, compliance, risks, and KPIs. Support onboarding, training, and resource transitions within projects. Participate in audits, inspections, CAPA, and non-conformance management activities. Coordinate activities with local partners and consultants when required. Profile Bachelor's degree in a scientific discipline or equivalent experience. 1-5 years of experience in Pharmacovigilance. Good understanding of local PV regulations and regulatory procedures. Strong organizational and communication skills. Proficiency in MS Office tools, particularly Excel and Word. Fluent English communication skills, both written and verbal. Experience with safety databases and MedDRA is an advantage. Why Join PLG? Work within an international and fast-growing life sciences organization. Collaborate with global experts in Pharmacovigilance and Regulatory Affairs. Benefit from continuous learning and development opportunities. Contribute to improving patient safety worldwide.
Key Responsibilities
Coordinate and oversee local pharmacovigilance activities for assigned safety projects. Ensure compliance with local and global PV regulations and timelines. Act as the primary operational contact for clients. Manage project tracking, reporting, and activity planning. Prepare, review, and maintain Pharmacovigilance Agreements (PVA), Safety Data Exchange Agreements (SDEA), and Technical Agreements. Monitor project quality, compliance, risks, and KPIs. Support onboarding, training, and resource transitions within projects. Participate in audits, inspections, CAPA, and non-conformance management activities. Coordinate activities with local partners and consultants when required. Profile Bachelor's degree in a scientific discipline or equivalent experience. 1-5 years of experience in Pharmacovigilance. Good understanding of local PV regulations and regulatory procedures. Strong organizational and communication skills. Proficiency in MS Office tools, particularly Excel and Word. Fluent English communication skills, both written and verbal. Experience with safety databases and MedDRA is an advantage. Why Join PLG? Work within an international and fast-growing life sciences organization. Collaborate with global experts in Pharmacovigilance and Regulatory Affairs. Benefit from continuous learning and development opportunities. Contribute to improving patient safety worldwide.