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Associate Director, Global Clinical Trial Management

Genmab - Utrecht
lifecycle of one or more clinical trials, from initial strategy through to Clinical Study Report (CSR) completion. This role involves leading cross-functional Clinical Trial Teams (CTT) and managing the trial budget to ensure
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Clinical Trial Manager

Genmab - Utrecht
essential to fulfilling our purpose. Clinical Trial Manager – Join Genmab’s Global Team At Genmab, we’re looking for a Clinical Trial Manager to join our dynamic Trial Strategy and Delivery team of over 75 passionate professionals
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Pharmaceutical Development Scientist / Technical Writer

Oxford Global Resources - Nijmegen
We are looking for a Pharmaceutical Development Scientist / Technical Writer. Your responsibility will be to optimize and validate manufacturing processes for pharmaceutical compounds intended for clinical trials. This
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Statistical Programmer (at the rank/grade of Technic...

Hku via Talent - Utrecht
Statistical Programmer (at the rank/grade of Technical Officer/Research Assistant I/II) in the Clinical Trials Centre (Ref: 524165) The Clinical Trials Centre (HKU-CTC) is a leading clinical trials management platform
FULL_TIME

PhD Deep learning for Quantitative MRI

Undisputed Muay via Talent - Amsterdam
routinely in cancer care. If we can improve the image quality of quantitative MRI, it can be used in clinical routine to select the optimal treatment for each patient, greatly improving treatment outcomes worldwide. Therefore, in
FULL_TIME

Executive Assistant - Corporate & Administrative Ser...

LabConnect via Talent - Swalmen
Executive Assistant - Corporate & Administrative Services Swalmen, Netherlands Req 364 Thursday, August 1, 2024 OverviewLabConnect improves lives by partnering with pharmaceutical and biotech companies, and clinical

Site Research Assistant

Iqvia via Talent - Venlo
coordinator, Research Assistant , nurse, medical assistant , other medical professionGood knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study -specific operating procedures, consent forms
CONTRACTOR

Site Research Assistant

Iqvia via Talent - Ede
Assistant , nurse, medical assistant , other medical professionGood knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study -specific operating procedures, consent forms, and study
CONTRACTOR

Clinical Research Coordinator

Iqvia via Talent - Zwolle
clinical research coordinator, Research Assistant , nurse, medical assistant , other medical professionGood knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study -specific operating
CONTRACTOR

Clinical Research Coordinator

Iqvia via Talent - Groningen
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
CONTRACTOR

Clinical Research Coordinator

Iqvia via Talent - Apeldoorn
clinical research coordinator, Research Assistant , nurse, medical assistant , other medical professionGood knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study -specific operating
CONTRACTOR

Clinical Research Coordinator

Iqvia via Talent - Nijmegen
clinical research coordinator, Research Assistant , nurse, medical assistant , other medical professionGood knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study -specific operating
CONTRACTOR

Clinical Research Coordinator

Iqvia via Talent - Utrecht
clinical research coordinator, Research Assistant , nurse, medical assistant , other medical professionGood knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study -specific operating
CONTRACTOR

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