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Clinical Quality Assurance Monitor

Chicago, IL
The Quality Assurance Monitor is responsible for ongoing monitoring of clinical trial data for local, investigator-initiated clinical trials, concentrating on data accuracy and completeness, protocol adherence, and toxicity and response review. 
 
Specific Responsibilities:
  • Reviews new protocols, specifically sections relating to registration procedures, records to be kept, eligibility criteria, and adverse event reporting
  • Verifies eligibility of and registers/randomizes participants to studies monitored by the DMC.
Minimum Qualifications:
  • Successful completion of a full 4-year course of study medical profession
  • 3-5 year’s prior experience coordinating or monitoring therapeutic clinical trials
  • Experience in staff education and training activities
 
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