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Clinical Research Coordinator

IQVIA - Amsterdam
hours per week and 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
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Clinical Research Coordinator

IQVIA - Apeldoorn
and 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
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Clinical Research Coordinator

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
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CRA for the EN)

Oxfordcorp - Rotterdam
maintenance of study monitoring plan, templates, trackers, study tools, and site-specific documents. Assists Clinical Study Manager (CSM) with development of human clinical protocol, investigational plan/brochure, SIV training
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Junior Clinical Research Associate (Junior CRA)

Oxfordcorp
Actively contribute to department results and goals Key Activities: Develop site visit plans, conduct Clinical Site Evaluation, Initiation, Monitoring and Close Out visits and prepare visit reports for project manager review
 60+ dagen geleden - Preview

Clinical Project Manager

Oxfordcorp
Oxford Global Resources is looking for a Global Project Manager based in Madrid. As the Global Project Manager you will actively lead the company and other stakeholder teams by combining deep clinical research
 60+ dagen geleden - Preview

Pharmacovigilance Manager

Oxfordcorp
Adverse Events are handled according to what is described in the Pharmacovigilance latest SOP : By preparing the SAE-form/e-SAE forms and guidelines and providing them to the Data Manager of the study . By checking that in
 60+ dagen geleden - Preview

Fair Market Value Specialist

Oxfordcorp
the company's Global Clinical Organization. Through coordination with Divisional Clinical Trial / Study Managers, the FMV and Budget Analyst conducts clinical trial site start-up activities related to the preparation of fair
 60+ dagen geleden - Preview

Country Study Start-up Specialist FR/EN)

Oxfordcorp
phase of clinical trials? Then this may be for you ! Job Description The Country Start-up Specialist will, for assigned sites/ study (s), ensure successful protocol level execution of start-up and regulatory activities
 60+ dagen geleden - Preview

Experienced CTA / Study Start-up Support Specialist

Oxfordcorp - Noord-Brabant
translations of study documents You coordinate and follow up site payments You are the single point of contact between clinical study team and project manager Requirements You have a bachelor degree with a minimum of
 60+ dagen geleden - Preview

Study Start-up Specialist

Oxfordcorp
setting. Responsibilities Conduct site engagement calls Conduct site evaluation calls or visits Collaborate closely with the global study teams, the local clinical team (Feasibility Manager , Oversight Manager
60+ dagen geleden - Preview

Study Start-Up Specialist

Oxfordcorp
One of the best pharmaceutical companies in the world is looking for a Study Start-Up Specialist in combination with Country Project Management responsibilities. Are you a (lead) Clinical Research Associate and want to gain
 60+ dagen geleden - Preview

Clinical Data Manager

Oxfordcorp
Description The Clinical Data Manager works under the hierarchical supervision of the Clinical Data Expert. The Clinical Data Manager reports on his/her activities and status of the study to the study team. The Clinical Data
 60+ dagen geleden
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