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Medical Science Liaison

Oxford Global Resources - Haarlem
expertise to drive clinical study recruitment efforts and accelerate progress for ongoing Phase II and III studies. Job Description In this role, you will be responsible for accelerating patient recruitment for Phase II and III
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Senior Principal Medical Writer remote

Yacht - Utrecht
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 regulatory documents across multiple therapeutic
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Lead Engineer Openshift

Schiphol Group - Schiphol
high quality airports’. Connecting your world Als Lead Engineer Openshift ben je primair verantwoordelijk en bevoegd om het platformteam te leiden bij technische ontwerpbeslissingen. Ook bewaak jij of de platform team
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Lab Analyst III

Icon Plc - Assen
What are your responsibilities? Preparation of clinical studies for the benefit of laboratory Practical translation of the clinical protocol to study specific instructions Maintain contact with internal and
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Lab Analyst I

Icon Plc - Assen
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the
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Lab Analyst I

Icon Plc - Assen
Assen ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to
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Lab Analyst III

Icon Plc - Groningen
Practical translation of the clinical protocol to study specific instructions Maintain contact with internal and external clients Efficient coordination of all your study related work in the laboratory Lead and
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Site Care Partner

Pfizer via Talent - Eindhoven
proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery. Manage Operational Study Management for one or more studies of limited complexity or a unique

Site Care Partner

Pfizer via Talent - Arnhem
proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery. Manage Operational Study Management for one or more studies of limited complexity or a unique

Site Care Partner

Pfizer via Talent - Capelle aan den IJssel
with the Study Manager. Work proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery. Manage Operational Study Management for one or more studies

Site Care Partner

Pfizer via Talent - Haarlem
proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery. Manage Operational Study Management for one or more studies of limited complexity or a unique

Site Care Partner

Pfizer via Talent - Utrecht
proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery. Manage Operational Study Management for one or more studies of limited complexity or a unique

Site Care Partner

Pfizer via Talent - Utrecht
proactively with Clinical Research Organizations (CRO) and data management functions to ensure alignment on data flow and timely delivery. Manage Operational Study Management for one or more studies of limited complexity or a unique