Clinical Research Coordinator

4 weeks ago


Evanston, United States Medasource Full time

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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