Sioux Falls, SD30+ days ago
Perform complex clinical procedures, including ECG, spirometry, sample collection, and vital signs • Phlebotomy required • Coordinate clinical research studies and ensure compliance with protocols and Good Clinical Practice (GCP) • Prepare study materials, set up equipment, and manage logistical activities • Recruit, screen, and orient volunteers while prioritizing their safety and well-being • Collect and accurately record clinical data in case report forms (CRFs) • Collaborate with investigators and monitors to resolve queries and maintain data quality • Act as a volunteer advocate and maintain a safe environment in line with Health and Safety policies. High School Diploma or equivalent education and experience Minimum 1 year of relevant clinical research experience (preferred) Working knowledge of clinical trials, GCP principles, and medical terminology Strong attention to detail and ability to build effective working relationships Advanced-level experience supporting site lead CRC with patient visits, data entry/query resolution, and prescreening physician referrals for eligibility Experience working in both research and clinical settings.