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Clinical Research Coordinator
4 weeks ago
Clinical Research Coordinator
Location: Evanston, IL
Hours: Monday-Friday, standard business hours
Required Travel: Some local travel required
What you will need:
- Education: Bachelor's degree preferred
- Certification: CCRP (or similar) preferred.
- Experience: At least two years of experience in coordinating clinical trials (experience with neurosciences/psychiatry/behavioral clinical trials highly preferred)
- Skills: Phlebotomy skills highly preferred (phlebotomy skills will be required as part of the job); organizational and problem-solving abilities, effective communication, basic computer skills; highly compliant with respect to research policies and procedures
What you will do:
- Coordinate and assist with multiple research studies (including in the areas of psychiatry, personalized medicine, outcome research, and family medicine)
- Prepare sites for conducting the study, including assisting PIs with feasibility assessments
- Develop Standard Operating Procedures, study forms, necessary database programs & data collection/entry strategies with applicable staff
- Review & prepare correspondence with the Endeavor IRB (initial submission, protocol amendments, adverse events, yearly progress reports
- Maintain regulatory documents as per sponsor & IRB protocols
- Screen subjects for eligibility
- Responsible for recruitment, coordination of care (in compliance with study protocol), and retention of research subjects
- Participate in the Informed Consent process
- Complete study activities as dictated by research protocols (including face to face and telephone assessments, medical records abstraction
- Responsible for specimen collection, processing, and shipping
- Coordinate & schedule appointments for diagnostic tests & procedures associated w/study protocols
- Ensure that study documents are complete, current, and filed
- Complete study close-out activities
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