Full responsibilities for clinical monitoring - line management of CRAs - ensures appropriate communication, regulatory documentation, and ongoing oversight - provide support for business development
Project Manager (PM)
Directing and leading project activities. Coordination, controlling and managing of clinical trial activities. Leading of study team.
Senior Clinical Research Associate (S-CRA)
Monitoring of clinical trials (bioequivalence studies, phase I studies, phase II-IV studies), logistic management, leading of study team.
Staff Associate
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