Assists investigators as coordinator of basic to complex clinical research study, managing and recording all phases of study protocol to ensure compliance
Job Summary
Assists investigators as coordinator of basic to complex clinical research study, managing and recording all phases of study protocol to ensure compliance.
Primarily recruits and enrolls study participants in a clinical setting, making determinations of eligibility and explaining study procedures to address participant/family concerns.
Includes rotating overnight on-call duties for an existing trauma trial, with additional compensation provided.
Matching Summary
Assists investigators as coordinator of basic to complex clinical research study, managing and recording all phases of study protocol to ensure compliance.
Salary
Base: $52,600.00 - $78,900.00 Annually; Bonus/Equity: Not specified; Benefits: Competitive health insurance, retirement plan, paid time off, tuition coverage
Skills & Requirements
Must-have
manage clinical research study phases
liaison with sponsors and participants
record study protocol compliance
recruit and enroll study participants
explain study procedures and consent
conduct lab duties and sample shipping
rotating overnight on-call duties
Nice-to-have
resolve IRB/protocol management issues
evaluate and interpret clinical data
prepare oral or written presentations
perform administrative tasks and literature reviews