Rochester Metro Area, NY
Bachelors degree in life sciences or health-related field with 4-6 years experience as a CRA in the pharmaceutical industry or for a Clinical Research Organization. Supporting Clinical Trial Research, or other clinical research service provider, or an equivalent combination of education and experience.
Summary: Under general direction, monitors the initiation and performance of clinical trials at external research sites to assure compliance with all study procedures and regulatory requirements. Serves as the primary liaison with the research site, tracks the progress of the study and resolves problems with the study execution. Conducts site qualification, site initiation, interim monitoring, and study termination visits. Assists with the development of study protocols, and identifies potential research sites. Upstate New York metropolitan area. HOME BASED position. Risk-based monitoring experience preferred.