Requirements: • Bachelors degree with 1 year of relevant experience in the life science industry OR • Associates degree with 2 years of relevant experience in the life science industry OR • High School Graduate and/or technical degree with minimum of 3 years relevant experience in the life science industry • Demonstrated knowledge of medical terminology • Demonstrated ability to use the following technology: Computers, Microsoft Office software, fax, copier, and multi-line telephone • Demonstrated ability to work in a fast-paced environment • Experience performing some clinical assessments, including but not limited to obtaining vital signs, EKGs, blood draws, processing, and shipping lab specimens • Excellent attention to detail, organization, and communication with varied stakeholders. • Coordinate with supervision duties for assigned clinical trials, including but not limited to study start-up, vendor management, subject recruitment, source document review and completion, protocol training, collection of regulatory documents, participant visits, timely data collection and documentation management, and reporting of adverse events, serious adverse events, and deviations, and monitoring visits and follow-up.