Clinical Study Manager

Manages the overall planning, conduct and progress of clinical studies, and clinical operation.  The CSM carry the responsibility for making sure the trial is planned and conducted under strict guidelines according to study protocol and regulation and according to company needs and timelines  REPORTS TO: Director of clinical and regulatory affairs


 Eperience as a study manager for medical device company or related field. Academic degree in life sciences. Extensive knowledge of ICH/GCP/ISO14155 regulations and guidelines CRA certificate Full working proficiency in English Experienced with Electronic Data Capture (EDC). Proficient in Microsoft Office including Excel, PowerPoint and MS Project.  Willing to travel abroad 15% of the time

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