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Freelance Medical Writer Life Sciences)
Yacht - Halfweg
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 - Rijnsaterwoude
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 4 uur geleden - Volledige vacature bekijken
Oxford Global Resources - Noord-Brabant
the clinical development plan, GCP, and SOP. Responsibilities Participate in Clinical Development activities for a study or a number of studies within a specific program or group of related programs.Contribute to60+ dagen geleden - Preview - Opslaan
Project Manager Clinical trials
Oxford Global Resources - Leiden
For one of our clients, an innovative pharmaceutical company located in Leiden, we are currently looking for a " Clinical Study Lead". Job Description Supporting the Development team in contributing to the clinical - Preview - Opslaan
(Junior) Clinical Trial Assistant EN or FR/EN or FR/EN)
Oxford Global Resources
Clinical Trial Assistant (NL/EN or FR/EN or NL/FR/EN) you will provide support for all study -related activities. Responsibilities Supports the execution of clinical studies Responsible for study start up activities60+ dagen geleden - Preview - Opslaan
Freelance Clinical Project Manager
Oxfordcorp
Do you have a degree in Life Sciences with experience in Clinical Research as Clinical Research Associate or as Clinical Project Manager and you're fluent in English? Then you may have your next project - Apply now60+ dagen geleden - Preview - Opslaan
Oxford Global Resources
Independently identify and follow up on adverse events and other safety issues related to the clinical study , and ensure timely communication of serious adverse events to the Clinical Study Manager ; Provide relevant, timely study 60+ dagen geleden - Preview - Opslaan
Oxford Global Resources
EN or NL/FR/EN) you will provide support for all study -related activities. Responsibilities: Supports the execution of clinical studies Responsible for study start up activities Tracks study related60+ dagen geleden - Preview - Opslaan
Oxford Global Resources - Utrecht
Clinical Research Manager - someone who sets up, standardizes and manages several clinical trials and clinical projects, done in-house and by several partner CRO's of this pharmaceutical and biotechnological, growing- Preview - Opslaan
Clinical Research Associate Manager EU - FR/EN
Oxford Global Resources
Job Description The CRA Manager EU will oversee implementation and execution of clinical trial(s) conducted in Europe to ensure study compliance, quality and on-time reporting. He/She will work closely with the in-house60+ dagen geleden - Preview - Opslaan
Oxford Global Resources - Noord-Brabant
This opportunity is open for Belgium-based Clinical Project Managers/ Clinical Study Lead with experience in IVD. Job Description As Clinical Project Manager , you manage overall clinical operations for assigned global60+ dagen geleden - Preview - Opslaan