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Freelance Medical Writer Life Sciences)
Yacht - Rijpwetering
the Medical Writer may include, but are not limited to, the following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical - Volledige vacature bekijken
Freelance Medical Writer Life Sciences)
Yacht
the Medical Writer may include, but are not limited to, the following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical 11 uur geleden - Volledige vacature bekijken
Freelance Medical Writer Life Sciences)
Yacht - Woubrugge
the Medical Writer may include, but are not limited to, the following: Works independently to write and edit clinical study reports, Investigator’s Brochures, Clinical Trial Results postings, annual reports, and other clinical - Volledige vacature bekijken
Opportunities Schmidt Consultancy
Schmidt Consultancy - Zutphen
Through their platform local study startup time of clinical trials is shortened and more patients can easily be included or referred. To ‘fill’ their platform with interesting trials for patients and oncologists, they are searching- Opslaan
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- Opslaan
Nine Zadelhoff Novartis past heel goed bij mij
Novartis
Nine van Zadelhoff werkt al 15 jaar bij Novartis, ze heeft het dan ook erg naar haar zin als clinical study manager (CSM). Ze werkt op de afdeling Trial Monitoring Operations (TMO), die toezicht houdt op de studies van60+ dagen geleden - Preview - Opslaan
Junior QA Assistant - Project Management
Oxford Global Resources - Leiden
required immunological assays. As a QA assistant you will supports one or more project leads in Clinical Immunology with activities relating to coordination of clinical study sample analysis Responsibilities Preparation- Preview - Opslaan
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 - Opslaan
Regulatory Affairs Administrator
Oxford Global Resources
Do you have an education in health-related or scientific discipline and a previous experience in Regulatory Affairs related to clinical trials environment ? Are you also fluent in English with the willingness to work in60+ dagen geleden - Preview - Opslaan
Icon Plc
2023-101258 Clinical Trial Support ICON Strategic Solutions Remote About the role This vacancy has now expired. Please see similar roles below... Voor één van z'n klanten is ICON op zoek naar een Study 60+ dagen geleden - Preview - Opslaan
Oxford 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 - Opslaan
Oxford Global Resources
varied job within the context of clinical trials. Function Description The administrative assistant provides support in a wide range of tasks related to the clinical trials run by our pharma client. Responsibilities60+ dagen geleden - Preview - Opslaan
Mriguidance - Utrecht
Are you interested in setting up, implementing and monitoring studies in hospitals around the world to make sure our methods are safe and effective? Unfortunately this vacancy is closed, thank you for your interest. If you l- Opslaan