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Vacatures pharmacovigilance

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Eortc Aisbl / Ivzw

The Pharmacovigilance Manager is responsible for all pharmacovigilance and safety activities for an EORTC study from study development until the archiving of the study. This includes management of all information concerning serious adverse events and serious adverse drug... 
2 maanden geleden
Sint-Lambrechts-Woluwe

Advanced S&S (Medical / Clinical)

 ...Pharmacovigilance Officer – Join a growing organization, in a role that comes with training and development opportunities! Location: Based close to Ghent but with options to work a few days a week from home, so commutable from Brussels, Antwerp and Bruges. My client... 
9 dagen geleden
Gent

HEALTH CARE MANAGEMENT

 ...verification of SPC, PIL and packaging materials Implementation of labelling of marketed products following approval Support for pharmacovigilance activities Assistance in SOP writing Follow-up of legislation Development of expertise in specific areas such as nutrients... 
4 dagen geleden
1831 Diegem

Ausy , a Randstad Company

 ...asset Strong initiative, pragmatic and problem solver Experience in other domains: medical writing, Regulatory Affairs or Pharmacovigilance Accurate & efficient: concern for quality, compliance and consistency Good communicator & team player Offer A... 
7 dagen geleden
1910 Kampenhout

Synergie Belgium nv

 ...verification of SPC, PIL and packaging materials Implementation of labelling of marketed products following approval Support for pharmacovigilance activities Assistance in SOP writing Follow-up of legislation Development of expertise in specific areas such as nutrients... 
1 dag deleden
1831 Diegem

Experis

 ...regulatory dossiers/data-packages in order to meet the submission timelines · Ensure that all regulatory aspects on the product safety/Pharmacovigilance and commitments/obligations to Authorities are closely monitored and fullfilled · Prepare cover letters, application forms,... 
15 dagen geleden
Provincie West-Vlaanderen

Experis

 ...regulatory dossiers/data-packages in order to meet the submission timelines · Ensure that all regulatory aspects on the product safety/Pharmacovigilance and commitments/obligations to Authorities are closely monitored and fullfilled · Prepare cover letters, application forms,... 
1 dag deleden
1300 Waver

SIRE Life Sciences®

 ...PIL en verpakkingsmaterialen; • Implementatie van etikettering voor op de markt gebrachte producten; • Ondersteuning voor pharmacovigilance; • Assisteren bij het schrijven van SOP's; • Follow-up en interpretatie van de wetgeving; • Ontwikkeling van expertise gericht... 
6 dagen geleden
België

Keyrus Biopharma

 ...better From early- to late-stage drug development, our range of services includes Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical... 
25 dagen geleden
België

Keyrus Biopharma

 ...better From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical... 
14 dagen geleden
Provincie Waals-Brabant

UCB S.A.

 ...immunology/neurology products and projects and their alignment and communication to internal (R&D, marketing, manufacturing, pharmacovigilance, quality assurance, regulatory affairs, and legal) and external (healthcare professionals, patients, advocacy groups, etc.) stakeholders... 
6 dagen geleden
Brussel

Keyrus Biopharma

 ...better From early- to late-stage drug development, our range of services includes: Project Management, Clinical Operations, Pharmacovigilance, Quality Assurance (GxP), Regulatory Affairs Strategy & Support, Data Management, Medical Review & Coding, Biostatistics, Medical... 
19 dagen geleden
Provincie Waals-Brabant

Planet Pharma Staffing Limited

 ...Monitoring, Clinical Project & Program Management, Clinical Programming & Data Management, Biostatistical Analysis & Reporting, Pharmacovigilance, Medical Writing, Regulatory Affairs, Quality Assurance and Validation. CHICAGO | BOSTON | SAN DIEGO | RTP | LONDON |... 
7 dagen geleden
België

UCB S.A.

 ...Safety Physician Location:  Braine L'alleud, Walloon Brabant, Belgium Job Function:  Drug Safety & Pharmacovigilance Job ID:  64943 Drug Safety Physician - Belgium UCB – Inspired by patients. Driven by science. Help us... 
12 dagen geleden
1420 Eigenbrakel

Covance

 ...one sponsor. Whether your specialization is in clinical monitoring, clinical project management, data management, biometrics or pharmacovigilance Covance has an FSP opportunity to match your area of expertise. Each FSP offers a unique opportunity to be a part of the... 
2 dagen geleden
Brussel

Keyrus Biopharma

 ...keystone for Keyrus Biopharma’s success Clinical & Business operations Regulatory Affairs Biometry Quality Assurance Pharmacovigilance Medical&Scientific Writing Medical Affairs Health Economics/Epidemiology Manufacturing/supply chain   So if... 
10 dagen geleden
Brussel

Medical Placement

 ...supervision médicale globale des études cliniques, participation aux réunions de mise en place d’études, supervision des activités de pharmacovigilance, revue des rapports d’études, rédaction de documents à visée règlementaire • Participation à la rédaction et à la revue des... 
18 dagen geleden
Brussel

Galapagos

 ...guidance to the members of your team; interact with internal stakeholders (Biometrics, Development Operations, Medical Affairs, Pharmacovigilance, Procurement, Quality & Compliance) and external stakeholders (CROs, equipment and service providers, insurance brokers);... 
15 dagen geleden
Mechelen

Proclinical Staffing

 ...dossiers/data-packages in order to meet the submission timelines. Ensuring that all regulatory aspects on the product safety/Pharmacovigilance and commitments/obligations to Authorities are closely monitored and fulfilled. Preparing cover letters, application forms,... 
10 dagen geleden
1300 Waver

Merck Sharp & Dohme Corp

 ...and internal requests Support the data consumption of product information data to downstream users within Regulatory Affairs, Pharmacovigilance, Manufacturing, etc. Participate in ISO IDMP-related initiatives in the company Skills General experience: ~English is required... 
7 dagen geleden
Brussel