Vacatures 1381 tot 1390 van 1.554 (ontdubbeld 1.553)
Oxfordcorp
Brand team and contribute to marketing strategic planning aligned with the medical lead Provide support to other functions including Regulatory Affairs, Drug Safety, Market Access, Pricing and Outcomes Research and Clinical60+ dagen geleden - Preview
Project Manager Chemical Safety
Oxfordcorp - Utrecht
GMP/GDP richtlijnen en bewaak je alles op het gebied Regulatory Affairs met betrekking tot CMC. Verantwoordelijkheden CMC projecten managen; Contact stakeholders; Verzorgen CMC documentatie; Coordineren- Preview
Oxfordcorp
study conduct. Provide professional presentation of study materials for investigator/vendor or country operations meetings Liaise with sites and in house departments to ensure appropriate regulatory follow-up60+ dagen geleden
Vitestro - Utrecht
regulatory requirements are therefore paramount. A considerable part of your work will therefore be spent on reviews, testing, documentation and quality management. You will work frequently outside your comfort zone, with a lot of- Preview
CERTARA, Oss Assistant Accountant Europe
The Cmpny - Eindhoven
Certara accelerates medicines to patients, partnering with life science innovators. Together with their partners, they advance modern drug development with modeling and simulation, regulatory science, and market access- Preview
Global Resourcing - Sint Maarten
Description What can you expect? Reporting to the Group Chief Financial Officer, the successful candidate will lead and be responsible for Financial Reporting (Statutory, Regulatory , Tax and other), Consolidation, Accounting- Preview
Compliance Grid Connection Specialist
TenneT TSO via Monsterboard - Arnhem
regulatory policies, such as Grid Connection Codes; Transmission system planning and analysis, including studies in stability and electromagnetic transients (EMT), to support a variety of in- and external clients such asDerksenderks via Monster Worldwide - Venray
Quality department are located in Venray. The Quality department assures, throughout the distribution process, that all sold products comply to the regulatory requirements and to the high quality standards our client offers. ThisQC Support Supervisor (HLO) - Balans Selective BV
Nederlandse Artsenvereniging voor Neuraaltherapie via Monster Worldwide - Groningen
Functieomschrijving Your key responsibilities in this role consist of: The QC Support Supervisor is responsible for performance of the QC support team and timely output according regulatory requirements (cGMP(Junior) Clinical Trial Assistant EN or FR/EN or FR/EN)
Oxfordcorp
sites, including preparing and distributing Study File Binders and Site Initiation presentations/materials Ensures collection, review, track and provision of appropriate clinical documents to support regulatory and EC/IRB60+ dagen geleden - Preview