Dec 14, 2025
Are you an experienced Senior Clinical Research Associate with considerable clinical research monitoring experience? Are you based in Germany and looking for a new contract role? If so, we are keen to hear from you!
Our leading CRO client is recruiting for a Senior CRA to be based in Germany, performing and coordinating all aspects of the clinical monitoring and site management process.
This position is offered on a 12 month contract basis initially, working 32 hours per week.
Description:
Work in accordance with ICH Good Clinical Practices, FDA guidelines, local regulations and PPD Standard Operating Procedures
Conducts site visits to assess protocol and regulatory compliance and manages required documentation.
Responsible for ensuring that data will pass international quality assurance audits.
Represent our client in the global medical research community and develops and maintains collaborative relationships with investigational sites and client company personnel.
Will assist...
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Outside IR35
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CV-Library
United Kingdom
Contractor