Vacatures 51 tot 60 van 100
ads
- Volledige vacature bekijken
- Volledige vacature bekijken
- Volledige vacature bekijken
Yacht - Eindhoven
implant is designed to reduce the frequency and intensity of migraine attacks by delivering gentle electrical pulses to the nerves associated with the condition. The company is currently in the clinical stage of development. In- Volledige vacature bekijken
Ilionx - Zwolle
zowel elkaar als met de klant. Jouw manager zorgt hierin vooral voor een prettige werkomgeving waarin hij jouw persoonlijke ontwikkeling én de samenwerking met jouw collegas juist alleen maar zal aanmoedigen. Als voormalig- Volledige vacature bekijken
Pro Industry - Breda
As manual packaging operator you execute the clinical labelling and packaging process according to standard operating labelling and packaging activities are mainly executed in room temperature conditions, but some products- Volledige vacature bekijken
Contract Manager bij Clinical Trial Service
Nine Orange - Losser
video die we van deze baan hebben laten maken en kom alles te weten! Clinical Trial Service Kom alles te weten over ons bedrijf Wij zijn een Contract Research Organisatie (CRO) die al 30 jaar gespecialiseerd is in- Preview
Associate Director Dossier Development
CLS Services via Monsterboard - Leiden
technical eCTD sections to support Regulatory CMC dossier applications. Your responsibilities are: Co-ordinate and provide technical oversight for the generation of the CMC dossier of marketing and clinical trial submissionsNovartis
belang dat we niet alleen naar de vergoeding van één middel kijken, maar het grotere plaatje blijven zien.” Meer weten over wat het werk van Ronald zo waardevol maakt? Nine van Zadelhoff Clinical Study Manager “Ik60+ dagen geleden - Preview
Lead CRA , Oxford Global Resources
Oxford Global Resources
work on the frontline of communication with project stakeholders, ensuring the successful conduct of clinical trials in a variety of therapeutic indications. You will supervise study start-up and site management activities to60+ dagen geleden - Preview
Regulatory Affairs Specialist - Dossier Development
Oxford Global Resources - Leiden
responsible for all issues regarding CMC. Responsibilities Coordinate and provide technical oversight for the generation of the CMC dossier of marketing and clinical trial submission. Develop the technical eCTD sectionsAssistant Scientist - Bacterial Strain Development
Oxford Global Resources - Leiden
immunogenicity and/or efficacy. In addition, manufacturing processes are optimized and established, and the resulting clinical trial material is evaluated in human clinical studies. We are currently looking for an Assistant Scientist toOpportunities Schmidt Consultancy
Schmidt Consultancy - Zutphen
60% of the cancer patients desire to participate in clinical trials. Only 5% actually does. To bridge this gap our client makes clinical trial protocols direct, online and easy to find, available for oncologist and patientsOxford Global Resources
Ensure clinical trial management systems containing all country and site-specific information are maintained and kept current during start up and study maintenance. Manage translations needed for regulatory activities60+ dagen geleden - Preview
Oxford Global Resources - Rotterdam
maintenance of study monitoring plan, templates, trackers, study tools, and site-specific documents. Assists Clinical Study Manager (CSM) with development of human clinical protocol, investigational plan/brochure, SIV training- Preview
Derksenderks via Monster Worldwide - Leiden
cycle reviews. You assure the completeness of the Product Specification File and the Study File to facilitate certification of clinical trial materials by the Qualified Person. As QA Manager you participate and contribute to