Clinical Research Coordinator - Oncology

*MUST have previous Oncology and on-site direct patient interaction experience Job Title Clinical Research Coordinator II FSLA Classification Non-Exempt Reports to CRCManager Job Summary / Objective The Clinical Research Coordinator II is responsible for supporting the management and oversight of clinical trials. This role involves working closely with a team to ensure the smooth execution of research studies under the guidance of the Site Operations Manager. Essential Functions Overseeing Clinical Trials Ensure trouble-free running of clinical trials. Monitor study participants’ health throughout the trial. Compile reports summarizing the success or failure of drugs, technologies, or medical procedures. Oversee 3-4 trials. Data Collection and Analysis Collect data obtained from research. Communicate with study participants regarding study objectives. Monitor participant adherence to study rules. Collaboration and Compliance Liaise with laboratories. Monitor study compliance with protocols and ethical standards. Ensure adherence to regulatory requirements. Maintain research records, including case report forms and drug dispensation records. Direct specimen collection, labeling, storage, and transport. Logistics and Supplies Ensure all necessary equipment and supplies are in stock and functional. Education / Experience / Skills Education: Bachelor's degree preferred in health-related field. Experience: 2 years of experience in Clinical Research. Skills: Filing and accessing documents, Study Submission Assistant, Conduct Close out Visits. Stipend payments. Recruit, interview, screen, enroll, and randomize subjects. Collect medical history. Conduct study visits. EDC. Query resolution. AE/SAE documentation and reporting. Address protocol violations and deviations. Order supplies. Clinical Skills: Vital Signs. ECG. Working Conditions / Physical Demands Standard operating hours are Monday through Friday, 8:00 a.m. to 5:00 p.m. May be required to complete job-related tasks outside of that time frame in excess of a standard 40-hour work week. Requires prolonged walking, standing, some bending, stooping, and stretching. Requires hand-eye coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator, and other office equipment. Requires normal range of hearing and eyesight to record, prepare, and communicate appropriate reports. Travel Required As needed (travel to IM’s may be required). #J-18808-Ljbffr