Research Associate
vor 1 Woche
Are you an experienced Clinical Research Associate with considerable clinical research monitoring experience? Our leading CRO client is recruiting for a CRA to be based in Germany, performing and coordinating all aspects of the clinical monitoring and site management process.
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 project manager or clinical team manager on assigned projects and will take a lead role where required.
Will support the line manager to mentor, train and contribute to the development of junior clinical team members.
Education and Experience:
Degree in a science related field or, a certified health care professional, or equivalent certification/licensure from an appropriately accredited institution.
Considerable clinical research monitoring experience with a demonstrated high level of expertise in all aspects of clinical monitoring.
Demonstrated ability to evaluate medical research data and proficient knowledge of medical terminology.
Fluency in English and in the country's native language.
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