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...

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...

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...

Revolution Medicines is seeking an experienced EU Deputy QPPV to join our dynamic team and report to the QPPV. You will support the oversight, maintenance, and continuous improvement of our European pharmacovigilance system, ensuring compliance with EU pharmacovigilance legislation and GVP.As Deputy EU QPPV, you will stand in for the EU QPPV, maintain...

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...

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...

Pharming Group seeks a Senior Manager Clinical Quality Assurance to provide strategic and operational leadership for clinical quality and pharmacovigilance.Lees verder voor een volledig begrip van deze vacature en wat er nodig is om een succesvolle sollicitant te zijn.You will lead the CQA team, ensure independent GCP/GVP oversight, and drive risk-based...

The role:Lees verder om volledig te begrijpen wat deze baan vereist op het gebied van vaardigheden en ervaring. Bent u een goede match, solliciteer dan.The 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...

The roleGeïnteresseerd in deze functie? U vindt alle relevante informatie in de omschrijving hieronder.The 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,...

The RoleGeïnteresseerd in deze functie? U vindt alle relevante informatie in de omschrijving hieronder.The 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,...

Genmab is looking for a Senior Manager in Safety Data Management to join their Global Drug Safety and Pharmacovigilance department.Lees hieronder meer over de algemene taken die bij deze functie horen, evenals de vereiste vaardigheden.The successful candidate will have over 5 years of experience in the biotechnology or pharmaceutical industry, specifically...

Pharming is seeking a Senior Manager CQA to provide strategic and operational leadership for clinical quality and pharmacovigilance.Kandidaten dienen de tijd te nemen om alle onderdelen van deze vacature zorgvuldig te lezen. Gelieve snel te solliciteren.You will oversee GCP and GVP activities, work with cross-functional teams, and ensure compliance with...

OverviewAre 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 opportunity!...

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,...

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company’s RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor;...

DUPP Amsterdam, North Holland, NetherlandsAls u iets meer wilt weten over deze vacature, of overweegt te solliciteren, lees dan de volgende vacature-informatie.DUPP Amsterdam, North Holland, Netherlands6 days ago Be among the first 25 applicantsWinclove Probiotics / DUPP - Food RecruitmentRegulatory Affairs ManagerWith a creative, structured and...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an English to Spanish (LatAm) Life Sciences Linguist based in Netherlands. This role offers the opportunity to contribute to high-quality language solutions supporting global pharmaceutical, clinical research, and medical device...

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...

For the past 20 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...