Teams at Evolution Research Group

Supports Phase I-IV clinical trials by dispensing investigational medications, performing vital signs, venipuncture, ECGs, point-of-care testing, specimen processing, documentation, and sample shipment. Maintains compliance with research protocols, GCP, ICH guidelines, site procedures, safety requirements, and regulatory standards while working collaboratively in a clinical research unit.

Manages daily administrative, financial, recruiting, regulatory, and operational activities for clinical research sites. Coordinates study feasibility, budgets, contracts, affiliate physicians, patient recruitment, regulatory compliance, database support, staffing, payroll, and sponsor obligations. Supervises multiple departments and collaborates with clinical research coordinators to ensure efficient study initiation, enrollment, documentation, and execution in accordance with GCP, ICH, FDA, and company requirements.

Supports Phase I-IV clinical trials by preparing source documents, conducting vitals, ECGs, and phlebotomy, entering patient visit data, managing lab kits, processing and shipping specimens, completing protocol training, and performing general administrative tasks. Ensures compliance with study protocols, FDA regulations, GCP, ICH guidelines, and company procedures. Requires strong organization, communication, attention to detail, medical terminology knowledge, and willingness to work night shifts.