Vacatures 21 tot 30 van 157 (ontdubbeld 152)
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Freelance Principal Medical Writer remote Life Sciences
Yacht - Amsterdam
postings, annual reports, and other clinical regulatory documents across multiple therapeutic areas as assigned. Works with contract writers as needed for the timely delivery of assigned documents. Reviews clinical protocols- Volledige vacature bekijken
Oxford Global Resources - Amsterdam
Do you have a scientific background and a first experience in a regulatory or scientific area? Then this might be the job for you! Job description The- Volledige vacature bekijken
Interim Regulatory Affairs Manager
Derks & Derks B. V. - Ankeveen
Offer own responsibility in several RA-related projects assignment for the duration of at least 3 months a challenging and engaging work - Volledige vacature bekijken
More Recruitment via Monster Worldwide - Naarden
Regulatory Affairs department. The QA unit is responsible for maintenance of the Quality Management System which is ISO 9001:2015 certified. In addition the QA unit is responsible for the submission of batch records and product- Opslaan
Regulatory Affairs Officer Fulltime Parttime Vast
Derks & Derks - Diemen
Amsterdam 2 weken geleden geplaatst Referentienummer: WS/24-306-DD Derks & Derks Uitdagende rol binnen Regulatory Affairs vanwege een groeiend productportfolio. Aanbod werken in een dynamische- Preview - Opslaan
Clinical Statistician - per year Contract May
Oxfordcorp - Utrecht
Specialist, Process Engineer, Validation Engineer, QA (Quality Assurance) Officer, RA ( Regulatory Affairs ) Officer, Supervisor, Team Leader, Department Head, Laboratory Manager, Manager, Director, etc. Please contact us directly! - Preview - Opslaan
Regulatory Affairs Technician ( remote)
Oxfordcorp
Oxford Global Resources is looking for a Regulatory Affairs Technician to work in a 6 months project for an multinational pharmaceutical company located in Madrid. Functions Preparation, management, and follow up of60+ dagen geleden - Preview - Opslaan
Oxfordcorp
driven by good publication practice principles. Track and report Scientific Publications performance. Support internal stakeholders (PV, IP/Legal, Regulatory , Research, GMA, etc.) with scientific publications related60+ dagen geleden - Preview - Opslaan
Oxfordcorp
Our client, a pharmaceutical company based in Belgium is looking for a (Junior) Regulatory Affairs Specialist a to come on board and join their team. The successful candidate will be responsible for managing regulatory 60+ dagen geleden - Preview - Opslaan
Oxfordcorp - Noord-Brabant
budgets, resources, investigational sites, vendors and key project deliverables in compliance with SOPs, regulatory requirements and ICH/GCP guidelines. As Clinical Project Manager you are a member of the clinical & medical60+ dagen geleden - Preview - Opslaan
Oxfordcorp
Oxford Global Resources buscamos a un Regulatory Affairs para una empresa líder farmaceútica. Responsabilidades: Compilación y redacción de documentación CMC (Química, Fabricación y Controles) para las solicitudes de60+ dagen geleden - Preview - Opslaan
Expert Regional Dossier Publisher
Oxfordcorp
Publisher, you will work with the Global Regulatory Affairs and Clinical Safety organization, in the EMEA Regulatory Operations but will provide support to the RRO organization globally. You are responsible for publishing key60+ dagen geleden - Preview - Opslaan
Product Development Scientist Medical Devices
Oxfordcorp - Utrecht
statistical sampling plans and testing protocols to ensure product quality and performance. Review, assess, and revalidate quality assurance and regulatory affairs documents. Investigate root causes of manufacturing issues- Preview - Opslaan