Clinical Research

• Assist with and oversee the day-to-day operations of clinical trials and studies
• Independently abstracts and records all research subject data pertaining to the research protocol onto protocol-specific Case Report Forms (CRFs) and into clinical trials database
• Obtain study subject’s medical history and current medication information, reviews research protocol inclusion/exclusion criteria, and confirms eligibility of subject to participate in clinical trial
• Perform informed consent process or ensures that the informed consent process has occurred, is properly documented, and that informed consent form documents are filed
• Interview prospective subjects for a variety of research clinical trials and educate potential subjects on the details of the studies
• Schedule subject participation in research clinical trial, coordinating availability of necessary space, and clinical research support
• Collaborate with other clinical research team members, investigators, and hospital staff to ensure tests and procedures required by research protocols are performed and documented
• Meet with Monitors to respond to any questions of data validity and correct/revise data as appropriate; responds to queries from Sponsor
• Adhere to research regulatory standards

Head and Neck Clinical Research Coordinator

Clinical Research Manager – GI/GU/Sarcoma

Clinical Research Manager – GI, GU, Sarcoma