Motivated clinical research coordinator looking forward to developing into a clinical research associate. Qualified medical research professional experienced in many coordinating aspects of clinical trials, protocols, and participant relationships. Experienced in both medical practice and clinical research environments. Demonstrate strong working knowledge of ICH-GCP, company standard operating procedures, regulatory guidelines, protocols, and monitoring guidelines. Communicate effectively with colleagues, medical personnel, and study participants. Peak professionalism, adhering to a code of ethics and business standards. Experienced in multiple study areas, including diabetes, hypertension, gastrointestinal, autoimmune disorders, cardiovascular, renal, and Parkinson's.