pharmacovigilance

Working hours: 40 (possible to work from home 2 days), PV 20 hours & RA 20 hoursHeeft u de juiste vaardigheden en ervaring voor deze functie? Lees verder om erachter te komen en dien uw sollicitatie in.Department: MedicalReports to: Quality and Regulatory Affairs ManagerPosition SummaryAs Pharmacovigilance & Regulatory Affairs Officer you will supports the...

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...

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...

A pharmaceutical company in Almere, Netherlands is seeking a Pharmacovigilance & Regulatory Affairs Officer to support key safety and registration processes within a regulated environment.U kunt meer details krijgen over de aard van deze vacature en wat er van sollicitanten wordt verwacht door hieronder te lezen.The ideal candidate must be fluent in Dutch...

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...

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...

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...

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...

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...

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...

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...

pGenmab is looking for a Senior Manager in Safety Data Management to join their Global Drug Safety and Pharmacovigilance department. /ppThe successful candidate will have over 5 years of experience in the biotechnology or pharmaceutical industry, specifically in Drug Safety. Responsibilities include safety system management and collaboration with team...

ph3Overview /h3pAre you an enthusiastic Regulatory Affairs (RA) professional looking to work in an RA department located on the same premises as the production facilities for biological medicines? Do you want to play a meaningful role in the eradication of polio worldwide? Then this position at the RA department of Bilthoven Biologicals (BBio) is your...

ph3Overview /h3pAre you an enthusiastic Regulatory Affairs (RA) professional looking to work in an RA department located on the same premises as the production facilities for biological medicines? The RA department manages the regulatory dossiers of all BBio products and ensures that changes in the vaccine manufacturing process are assessed in terms of...

At uniQure, we are delivering on the promise of gene therapy and delivering hope for patients facing urgent unmet medical needs. Every role in our organization carries profound purpose; whether you're in research, operations, access, or support, your contributions impact patients. We're seeking passionate professionals who thrive in high-stakes environments,...

pPharming Group seeks a Senior Manager Clinical Quality Assurance to provide strategic and operational leadership for clinical quality and pharmacovigilance. You will lead the CQA team, ensure independent GCP/GVP oversight, and drive risk-based quality management across the product lifecycle. /ppYou will partner with Clinical Development, Medical Affairs,...

pPharming Group seeks a Senior Manager Clinical Quality Assurance to provide strategic and operational leadership for clinical quality and pharmacovigilance. You will lead the CQA team, ensure independent GCP/GVP oversight, and drive risk-based quality management across the product lifecycle. /ppYou will partner with Clinical Development, Medical Affairs,...

ph3The role /h3 pThe Senior Manager Clinical Quality Assurance (CQA) provides strategic and operational leadership for clinical and pharmacovigilance quality. The role is accountable for independent GCP and GVP oversight, a risk-based quality management approach, inspection readiness and the effective operation of the clinical quality management system, in...

ph3The role /h3 pThe Senior Manager Clinical Quality Assurance (CQA) provides strategic and operational leadership for clinical and pharmacovigilance quality. The role is accountable for independent GCP and GVP oversight, a risk-based quality management approach, inspection readiness and the effective operation of the clinical quality management system, in...