CLINICAL RESEARCH COORDINATOR OPPORTUNITY IN GRAYSLAKE, IL!
**MUST HAVE RESEARCH EXPERIENCE**
Clinical Research Coordinator Job Description:
Coordinates all aspects of the study including recruitment, consent, screening, scheduling, tracking and provides study updates to study participants throughout the conduct of the study
May collect and enter data into study case report forms and/or electronic data capture system and respond to queries in a timely manner.
Submits or partners with a regulatory coordinator to submit study related documents, study protocols and study protocol amendments to the IRB per policy and procedure
Ensures procedural documentation is accurate, complete, and in compliance with institutional, local, state and federal guidelines and regulations related to clinical research.
May collect, process and ship potentially biohazardous specimens
May administer more complex structured tests and questionnaires according to research study protocols. May utilize study-related technology and equipment as part of assessment procedures.
Provide ongoing study status updates, responds to questions and may create summary report(s) for distribution to PI, Administrator, Office of Research Affairs, Sponsor and Compliance throughout the conduct of the study
Organize and participate in auditing and monitoring visits
Requirements:
Bachelor's/Associate's degree or equivalent experience
2+ years of experience in Clinical Research
Details:
Location: Grayslake, IL
Pay: $55K-$75K (Dependent on years of experience)
Hours: Monday - Friday; Normal Business Hours (Onsite 5 Days a Week)
Duration: 6 month Contract to Hire (1,040 hours) - contracted probationary period into direct hire / permanent position