Other duties as assigned or required by management.♼oordinate with external reviewers to ensure compliance with regulatory agency requirements and company policies and procedures. ♺ssist in conducting post-study audits as needed. ♺ssist in conducting phase III studies as needed. ♺ssist in conducting phase I/II studies as needed. ♺ssist in conducting post-approval studies as needed. ♺ssist in conducting pre-approval studies as needed. ♼oordinate with external reviewers to ensure study compliance with regulatory agencies. ♼oordinate with external review groups to ensure study compliance with regulatory agencies. Manage and maintain all clinical study files and clinical databases.Responsibilities: ♼oordinate the clinical research activities at the clinical site, including but not limited to: recruitment, retention, data management, data entry and reporting. As a company, we are in a high growth mode and those with clinical research experience, if interested, will be considered for the Site Director’s role that is currently open. This position will be responsible for coordinating the clinical research activities at the clinical site. The Clinical Research Coordinator will work closely with the Director of Clinical Research and the clinical staff to ensure that all study requirements are met. The ideal candidate will have a passion for helping people, a desire to learn and a willingness to take on new responsibilities. IC Research is seeking a Clinical Research Coordinator to join our team at our research site in Sanford, FL.
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