Clinical Research Technician / Assistant (underfill)

About the position Responsibilities • Actively recruit potential participants for clinical studies through outreach and database searches. • Coordinate pre-screening, eligibility assessment, informed consent, and enrollment of study participants. • Provide participants with information regarding study protocols, ensuring understanding of requirements, risks, and benefits. • Maintain regular contact with study participants to monitor adherence and manage concerns. • Conduct follow-up visits as specified in the study protocol, documenting participant health status and compliance issues. • Accurately enter patient data into study databases, ensuring data integrity and completeness. • Conduct quality control checks and resolve discrepancies in data entries. • Prepare and submit IRB applications, renewals, and protocol deviation reports. • Monitor regulatory timelines and ensure compliance with institutional and federal regulations. • Schedule and coordinate study-related meetings and assist with the development of study protocols. Requirements • Associate degree in Health Science or equivalent experience. • Minimum 1 year of directly related experience in clinical research and clinical trials or an advanced degree in a health-related area. • Minimum 3 years of human subject experience in clinical, lab, or health regulations. Nice-to-haves • Understanding of medical terminology and experience in a large complex health care setting. • Ability to effectively communicate with staff and faculty of all levels. • Knowledge of university policies and procedures. • Bachelor's degree in Health Science or equivalent experience. Benefits • Excellent medical, dental and vision coverage effective on the first day. • 2:1 Match on retirement savings.