pharmacovigilance

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...

uniQure is seeking a Senior Director of Safety Operations to lead the pharmacovigilance (PV) function globally. You will design, implement and optimize the PV system, ensure regulatory compliance and drive cross‑functional collaboration with Clinical Development, Operations, Medical Affairs, Quality and IT to support life‑changing therapies.The role...

ppbWorking hours: /b 40 (possible to work from home 2 days), PV 20 hours RA 20 hours /p pbDepartment: /b Medical /p pbReports to: /b Quality and Regulatory Affairs Manager /p h3Position Summary /h3 pAs Pharmacovigilance Regulatory Affairs Officer you will supports the daily activities of Pharmacovigilance (PV) and Regulatory Affairs (RA) within a regulated...

Shionogi Europe is seeking a Senior Safety Physician to join our European Drug Safety team. The role involves hands-on pharmacovigilance across development and marketed products, providing medical expertise and regulatory input in an international setting.You will contribute to signal management, regulatory responses, and safety studies, working with...

ppbWorking hours: /b 40 (possible to work from home 2 days), PV 20 hours RA 20 hours /p pbDepartment: /b Medical /p pbReports to: /b Quality and Regulatory Affairs Manager /p h3Position Summary /h3 pAs Pharmacovigilance Regulatory Affairs Officer you will supports the daily activities of Pharmacovigilance (PV) and Regulatory Affairs (RA) within a regulated...

pProPharma Group seeks a Senior Pharmacovigilance Consultant, Alliance Management, to implement and maintain alliance services for clients, including LPPV roles, LPPV networks, PSMF management, and SDEA/PVSA drafting. /ppThe role involves coordinating cross-functional teams, supporting PV governance, and ensuring regulatory alignment across UK/EU while...

ppThe Senior Pharmacovigilance Consultant, Alliance Management, implements and maintains Alliance Management services for ProPharma clients, such as covering the role of a Local Contact Person Responsible for Pharmacovigilance (LPPV), coordinating LPPV networks, maintaining the Pharmacovigilance System Master FIle (PSMF), managing Pharmacovigilance Services...

The Senior Pharmacovigilance Consultant, Alliance Management, implements and maintains Alliance Management services for ProPharma clients, such as covering the role of a Local Contact Person Responsible for Pharmacovigilance (LPPV), coordinating LPPV networks, maintaining the Pharmacovigilance System Master FIle (PSMF), managing Pharmacovigilance Services...

pProPharma Group seeks a Senior Pharmacovigilance Consultant, Alliance Management, to implement and maintain alliance services for clients, including LPPV roles, LPPV networks, PSMF management, and SDEA/PVSA drafting. /ppThe role involves coordinating cross-functional teams, supporting PV governance, and ensuring regulatory alignment across UK/EU while...

puniQure is seeking a Senior Director of Safety Operations to lead the pharmacovigilance (PV) function globally. You will design, implement and optimize the PV system, ensure regulatory compliance and drive cross‑functional collaboration with Clinical Development, Operations, Medical Affairs, Quality and IT to support life‑changing therapies. /ppThe role...

The Role & DepartmentAs a Senior Manager, Safety Data Management, you will become part of the Global Drug Safety and Pharmacovigilance (GDSPV) department, where you will be responsible for safety data management activities including but not limited to configurations and maintenance of safety systems, generation of complex ad-hoc reports, and implementation...

A pharmaceutical company in Almere, Netherlands is seeking a Pharmacovigilance Regulatory Affairs Officer to support key safety and registration processes within a regulated environment. The ideal candidate must be fluent in Dutch and English and have 1-3 years of experience in pharmacovigilance or regulatory affairs. Responsibilities include recording...

A pharmaceutical company in Almere, Netherlands is seeking a Pharmacovigilance Regulatory Affairs Officer to support key safety and registration processes within a regulated environment. The ideal candidate must be fluent in Dutch and English and have 1-3 years of experience in pharmacovigilance or regulatory affairs. Responsibilities include recording...

ph3The Role Department /h3pAs a Senior Manager, Safety Data Management, you will become part of the Global Drug Safety and Pharmacovigilance (GDSPV) department, where you will be responsible for safety data management activities including but not limited to configurations and maintenance of safety systems, generation of complex ad-hoc reports, and...

Join us on our exciting journey! IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics, and human...

pIQVIA is seeking a Medical Safety leader to oversee pharmacovigilance activities across clinical development and post-marketing programs. The role requires MD or equivalent, deep pharmacovigilance knowledge, and proven leadership in multinational teams. /ppResponsible for medical review of safety data, regulatory submissions, and safety governance, you will...

pIQVIA is seeking a Medical Safety leader to oversee pharmacovigilance activities across clinical development and post-marketing programs. The role requires MD or equivalent, deep pharmacovigilance knowledge, and proven leadership in multinational teams. /ppResponsible for medical review of safety data, regulatory submissions, and safety governance, you will...

TheLead Commercial Qualityensures that commercial distribution activities are conducted in full compliance with EU Good Distribution Practice (GDP) and EU Good Pharmacovigilance Practice (GVP), while supporting business growth through pragmatic, risk-based governance. The position enables the compliant supply of prescription products, particularly allergen...

Senior Safety Physician Why join Shionogi? At Shionogi, safety is at the heart of what we do. We are looking for an experienced (Senior) Safety Physician to join our European Drug Safety team and play an important role in our pharmacovigilance activities across both clinical development and marketed products. This is a hands‑on position with broad exposure...

The Lead Commercial Quality ensures that commercial distribution activities are conducted in full compliance with EU Good Distribution Practice (GDP) and EU Good Pharmacovigilance Practice (GVP), while supporting business growth through pragmatic, risk-based governance. The position enables the compliant supply of prescription products, particularly allergen...