Clinical Trials Coordinator
: Job Details :

Job Description This position is responsible for coordinating clinical research studies on human subjects. Responsible for subject recruitment, follow-up, data management, detailed record keeping and regulatory compliance, report writing, and correspondence with investigators, IRBs, and regulatory authorities. Responsible for the new submission of protocols with subsequent amendments. Some participation in protocol writing, and initial and continuing education for Good Clinical Practice compliance. Qualifications • Bachelor's Degree in scientific field required. RN preferred. • Clinical research certification (such as CCRC, CCRP, CRA, IATA) preferred. If not yet certified, expected certification within 6-12 months of hire date. • Human Research Subject Protection and Good Clinical Practice Certification • OSHA training for handling hazardous biologic and chemical materials