Highly qualified medical research professional skilled in all aspects of clinical trial coordination, protocols, and participant relationships. Experienced in performing protocol specific tasks such as vitals signs, ECGs, phlebotomy and rater assessments. Demonstrates strong working knowledge of ICH-GCP, company standard operating procedures, regulatory guidelines, protocols and monitoring guidelines. Communicates effectively with medical personnel, colleagues, and study participants. Experienced in multiple study areas, including Alzheimer's disease, Parkinson's disease, Diabetes, Migraines, Cardiovascular disease and Women's studies. Organized and dependable candidate successful at managing multiple priorities with a positive attitude.
ICH Good Clinical Practice (GCP) | Cardiopulmonary Resuscitation (CPR) | Health Insurance Portability and Accountability Act (HIPAA) |