Clinical Research Coordinator II Position Available In Fulton, Georgia

Job Title:

Clinical Research Coordinator II Job Description The Clinical Research Coordinator II coordinates, implements, and evaluates clinical research trials, studies, and projects. The role involves providing direction in the development of research protocols, recruiting and screening potential study participants, and developing and conducting patient and family education. Responsibilities Independently manage significant and key aspects of Oncology related trials including one or more small trials or research projects. Operate as Oncology Research Coordinator in support of specified Oncology disease group(s). Perform required patient consents. Train and provide guidance to less experienced staff. Oversee data management for research projects. Interface with research participants and resolve issues related to study protocols. Authorize purchases for supplies and equipment maintenance. Determine effective strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. Periodically audit operations, including laboratory procedures, to ensure compliance with applicable regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor IRB submissions and respond to requests and questions. Interface with study sponsors, monitor and report SAEs, and resolve study queries. Provide leadership in determining, recommending, and implementing improvements to policies/processes. Assist in developing grant proposals and protocols. With appropriate credentialing and training, perform phlebotomy, specimen collection, or diagnostics. May perform some supervisory duties. Perform related approved responsibilities as required. Essential Skills Good Clinical Practice (GCP) Patient consenting CRC (Certified Research Coordinator) SAE reporting 2+ years of CRC experience in oncology or interventional drug trials in other therapeutic areas Experience reporting AE/SAE within NIH and Pharma funded trials where drugs were dispensed CCRC (Certified Clinical Research Coordinator) CRF (Case Report Form) ICF (Informed Consent Form) Additional Skills & Qualifications 2+ years of clinical research experience Bachelor’s degree Work Environment This position is office-based in a hospital clinic setting, with a Monday-Friday 8-5 work schedule. The coordinator may be asked to travel to downtown ATL sites due to their high enrolling locations. The role offers the opportunity to be part of cutting-edge oncology research and therapies, and to work closely with top investigators in the field.