Vacatures 121 tot 128 van 128
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IQVIA - Nijmegen
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies- Volledige vacature bekijken
IQVIA - Utrecht
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies- Volledige vacature bekijken
IQVIA - Zwolle
is expected to last approximately 12-17 months. The successful candidate will be responsible for supporting a clinical research study and maintaining a safe study environment in accordance with health and safety policies- Volledige vacature bekijken
Oxfordcorp
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
Oxfordcorp
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
Oxfordcorp - 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
Oxfordcorp
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
Oxfordcorp - 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
Oxfordcorp
develop yourself as a Clinical Trial Manager as the opportunity offers a headquartered role. Job Description The CPM/ Clinical Study Manager , in concert with the COM ( Clinical Operations Manager ), is accountable for achieving60+ dagen geleden - Preview - Opslaan
Oxfordcorp
European multi-country clinical studies. Responsibilities Management of European multi-country clinical studies Develop, review and manage appropriate study documentation in the trial master File (TMF) Periodically60+ dagen geleden - Preview - Opslaan