Clinical Research Coordinator


North Chicago, IL

Industry: Biotech/Pharma


Not Specified years

Posted 381 days ago

  by    Nency Patel

Managing clinical documents for multi-site studies, prioritize multiple tasks and/or projects with limited supervision.

Ideal candidates will possess strong organizational capabilities and strong interpersonal skills, along with excellent written and verbal skills.

Ensure documents are compliant with SOPs and regulatory requirements.

Review essential/critical documents for completeness and accuracy

Bachelor’s degree is required.

Must be computer literate.


Job duties include managing the Trial Master File (TMF), ensuring documents maintained in the file are appropriate and the content of those documents is accurate, complete and consistent with Client SOPs and regulatory requirements.

A Bachelor’s degree is required.

Managers are interested in candidates that have some experience of clinical trials/clinical research.

Candidates with lab/experiment research are not a fit for these positions, nor are candidates with MDs.

Candidates must be computer literate.