Senior CRA: Phase II-III Monitoring & Site Initiation
Resourcing Group
Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a CRA in Netherlands. The role is sponsor dedicated via the CRO Job Overview Monitoring clinical studies in phases II-III Assuring adherence to Good Clinical Practices, investigator integrity, and compliance with all study procedures. Identification, qualification and initiation of investigators and their sites. Supervising study conduct according to GCP requirements and all applicable laws. Key Requirements Bachelor degree in life-science Min 18 months experience as CRA / Clinical Research Associate within a CRO, Pharma, Biotech Experience in commercial studies Experience with site initiation, site close out Experience in clinical studies phase II-III
FTE: 1.0
if you have difficulty in applying for this role please email us on View email address on click.appcast.io #J-18808-Ljbffr Resourcing GroupVacancy posted 3 days ago
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