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CRA Sponsor Dedicated Sweden

Resourcing Life Science

Company Description 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 Clinical Research Associate/ CRA sponsor dedicated, Home Based in Sweden in one of the major cities. 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 1 year monitoring experience as CRA within a CRO, Pharma, Biotech in Sweden Experience in commercial studies Experience with site initiation, site close out Experience in clinical studies phase II-III Fluent English & Swedish Excellent communication skills A full clean drivers license

FTE: 1.0

#J-18808-Ljbffr Resourcing Life Science

Vacancy posted 3 days ago
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