Beaumont Health System Clinical Research Coord II in Royal Oak, Michigan
Clinical Research Coord II Req #: 30100152 Category: Business Ops Facility: Research Building Department: ORSX FISCHJ ORTHO CLIN RSCH Schedule: Full time Shift: DaysHours: 8:00 am - 4:30 pm; Hours and Days may vary as needed Job Details:The Clinical Research Coordinator II (CRC II) is responsible for protocol coordination, including subject recruitment, enrollment, implementation, and follow-up of appropriate research protocols.Duties: CRCII study personnel promote good clinical practice in the conduct of research possessing knowledge of federal regulations and guidance documents for the conduct of clinical trials and human subject protection. Participates in subject screening, recruitment, enrollment and follow-up procedures, pre-study preparation, problem solving and maintenance of clinical trials. Collection, processing and shipping of research specimens, including blood draws with appropriate training. Documents all study-related procedures and events utilizing CRFs or EDC, participates in monitoring visits, reviews CRF with sponsor and handles data queries as appropriate. This position will be required travel to and from Physician Private Practice Office and hospital. Prepare for and participate in sponsor and external regulatory audits and departmental audits, including review of study and regulatory documents for accuracy and completeness. BLS Certification required. National Research Certification (SoCRA or ACRP) required.Preferred: Orthopedic experience Research/regulatory experience preferred.Phlebotomy skills prior to hire highly preferred.ACKNOWLEDGEMENT OF EMPLOYMENT UNDER RESEARCH GRANTBeaumont Health is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, , gender identity, orientation, age, status as a protected veteran, or status as a qualified individual with a disability.