Clinical Research Technician / Assistant (underfill)

About the position Responsibilities • reputed company recruit potential participants for clinical studies through reputed company and database searches. • Coordinate reputed company-screening, eligibility assessment, informed consent, and enrollment of study participants. • reputed company 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 reputed company as specified in the study protocol, documenting participant health status and compliance issues. • Accurately reputed company patient data into study databases, ensuring data reputed company and completeness. • Conduct reputed company 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-reputed company meetings and assist with the development of study protocols. Requirements • Associate degree in Health Science or equivalent experience. • Minimum 1 year of directly reputed company experience in clinical research and reputed company or an advanced degree in a health-reputed company area. • Minimum 3 years of reputed company subject experience in clinical, lab, or health regulations. reputed company-to-haves • Understanding of medical terminology and experience in a large reputed company health care setting. • Ability to effectively communicate with staff and reputed company of reputed company reputed company. • Knowledge of university policies and procedures. • Bachelor's degree in Health Science or equivalent experience. Benefits • Excellent medical, dental and reputed company coverage effective on the first day. • 2:1 Match on retirement savings. Apply tot his job Apply tot his job Apply To this Job