Emplois : pharmacovigilance manager

At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. Qualified Person Responsible for Information and...

Notre partenaire est un acteur international de premier plan dans les services réglementaires et de pharmacovigilance pour l’industrie pharmaceutique et des dispositifs médicaux. Il accompagne des laboratoires internationaux dans l’ensemble des activités liées à l’approbation, au développement et au maintien des produits sur le...

An international pharmaceutical consultancy has new big projects coming in. To support this, they need to grow the Pharmacovigilance team with a PV Manager. They are a big global company with pharmacovigilance expertise and very good contacts with multiple clients to ensure a good flow of incoming projects. You will work together with an international team...

**Make your mark for patients** To strengthen our **Global** **Quality Assurance** department, we are looking for a talented professional to fill the position of: **Evidence Quality Lead – Braine l’Alleud, Belgium.** **About The Role** As part of the UCB Quality organization, the Evidence Quality Lead (EQL) actively enables compliant Research,...

**Introductie** Onze klant is een van de toonaangevende dienstverleners voor de farmaceutische industrie wereldwijd en is gespecialiseerd in alle aspecten van de goedkeuring van geneesmiddelen en medische hulpmiddelen, marktontwikkeling en alle activiteiten met betrekking tot effectief productonderhoud. **Jobomschrijving** De Manager Local...

**Introduction** For our client, a veterinary medicines and feeds company we are looking for a Veterinary Regulatory and Quality officer. Check this great opportunity **Job Description** As a Regulatory Affairs & Pharmacovigilance Specialist, you will play a key role in safeguarding the quality, compliance, and safety of veterinary medicinal products...

BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate interest in fighting cancer. *Qualified Person Responsible for Information...

A global biopharmaceutical company is seeking a Benefit Risk Lead to support patient safety initiatives. This role involves analyzing data, implementing risk management strategies, and collaborating with diverse teams. Candidates should hold a Physician's degree and possess experience in pharmacovigilance and safety writing. Strong project management and...

Planet Pharma are currently partnered with a global pharmaceutical company and we are actively seeking a Clinical Research Associate I to join the business on a permanent basis in Belgium. Key Responsibilities: Monitor clinical trial sites to ensure studies are conducted in compliance with ICH-GCP, protocol requirements, and regulatory guidelines. ...

Make your mark for patientsAre you passionate about advancing patient safety and drug development? Join our Patient Benefit Risk and Medical Safety team as a Benefit Risk Lead , where your analytical mindset and collaborative and proactive attitude will help deliver safe and effective treatments. This role is based in our Brussels office in Belgium or Slough...

Planet Pharma are currently partnered with a global pharmaceutical company and we are actively seeking a Clinical Research Associate I to join the business on a permanent basis in Belgium. Key Responsibilities: Monitor clinical trial sites to ensure studies are conducted in compliance with ICH-GCP, protocol requirements, and regulatory guidelines. ...

Planet Pharma are currently partnered with a global pharmaceutical company and we are actively seeking a Clinical Research Associate I to join the business on a permanent basis in Belgium. Key Responsibilities: Monitor clinical trial sites to ensure studies are conducted in compliance with ICH-GCP, protocol requirements, and regulatory guidelines. ...

Make your mark for patients Are you passionate about advancing patient safety and drug development? Join our Patient Benefit Risk and Medical Safety team as a Benefit Risk Lead , where your analytical mindset and collaborative and proactive attitude will help deliver safe and effective treatments. This role is based in our Brussels office in Belgium or...

Make your mark for patientsThis role is based in our Brussels office in Belgium or Slough office in the United Kingdom.About The RoleYou will be working in a team that leads the strategic planning, delivery, and communication of benefit‐risk assessments and risk management strategies for our medicines. Your focus will be on supporting clinical development...

A global biopharmaceutical company in the United Kingdom is seeking a safety-focused professional to join their team. You will lead risk management strategies and support clinical development by evaluating benefit-risk outcomes and emerging safety concerns. The candidate should possess an MD and have experience in pharmacovigilance. The position offers a...

Planet Pharma are currently partnered with a global pharmaceutical company and we are actively seeking a Clinical Research Associate I to join the business on a permanent basis in Belgium.Key Responsibilities:Monitor clinical trial sites to ensure studies are conducted in compliance with ICH-GCP, protocol requirements, and regulatory guidelines.Perform site...

Planet Pharma are currently partnered with a global pharmaceutical company and we are actively seeking a Clinical Research Associate I to join the business on a permanent basis in Belgium. Key Responsibilities: Monitor clinical trial sites to ensure studies are conducted in compliance with ICH-GCP, protocol requirements, and regulatory guidelines. ...

We are seeking Clinical Research Associates at Level I or Level II to support oncology clinical trials with a high level of involvement and ownership. This role is ideal for CRAs who want to move beyond pure monitoring and take responsibility across the full study lifecycle.Key Responsibilities: As a CRA, you will be responsible for end-to-end site and study...

Position: Senior Drug–Device Combination Documentation ExpertLocation: On-site - Braine, BelgiumClient: BiotechType: 12 months contract initially - full-time (40hours per week)About the RoleSenior expert in drug–device combination product development, with a strong focus on autoinjector platforms.Strategic and hands-on role covering development,...