Clinical Research Coordinator 231772

job
  • Medix™
Job Summary
Location
Chicago ,IL
Job Type
Contract
Visa
Any Valid Visa
Salary
PayRate
Qualification
BCA
Experience
2Years - 10Years
Posted
15 Nov 2024
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Job Description
  • Conducts study start-up activities and prepares and maintains all regulatory documents required by sponsor and/or regulatory agencies.
  • Prepares protocols, informed consent documents, modifications, renewals and other necessary documents for review by the IRB and/or sponsor.
  • Coordinates study conduct with other departments to effectively implement clinical research projects; obtains required letters of support and/or approvals as needed (i.e. IBC, SRC, etc.) and protocol is followed.
  • Identifies and recruits eligible study subjects; conducts informed consent/assent process.
  • Arranges and conducts clinical research visits.
  • Conducts site qualifications, study initiation, monitoring and/or close-out visits.
  • Attends investigator meetings.
  • Abstracts data from medical records and enters medical information/data onto protocol specific case report forms, study flow sheets, and other required study forms; prepares abstracted/coded data for processing/analysis.
  • Creates and/or updates case report forms and/or source document templates.
  • Coordinates reimbursement of subjects.
  • Maintains inventory of supplies/equipment.
  • Prepares lab kits and requisitions prior to visits.
  • Collects specimens from subjects and processes specimens or works with Research lab to ensure samples are processed/sent out correctly.
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