The role involves assisting investigators by managing all phases of basic to moderately complex clinical research studies while ensuring strict compliance with regulatory agency requirements
Job Summary
The role involves assisting investigators by managing all phases of basic to moderately complex clinical research studies while ensuring strict compliance with regulatory agency requirements.
Candidates will be responsible for recruiting study participants, obtaining informed consent, and coordinating with the Principal Investigator, IRB, and sponsoring agencies.
The position offers competitive benefits including up to 22 days of vacation, health insurance packages, a retirement savings plan, and tuition coverage for employees and families.
Matching Summary
The role involves assisting investigators by managing all phases of basic to moderately complex clinical research studies while ensuring strict compliance with regulatory agency requirements.
Salary
Base: $47,400.00 - $71,200.00 annually; Bonus/Equity: Not specified; Benefits: Up to 22 days vacation, health insurance, 403(b) retirement match, tuition coverage
Skills & Requirements
Must-have
manages clinical study protocols
ensures regulatory compliance
recruits and enrolls participants
obtains informed consent
collects and analyzes clinical data
coordinates with IRB and sponsors
Nice-to-have
strong interpersonal communication skills
experience with OnCore systems
ability to work in patient care setting
organizational and time management skills
Key Requirements
Bachelor's degree or equivalent experience
Basic Life Support (BLS) certification with skills assessment