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Research Coordinator
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Full-time
- The Research Coordinator will screen, enroll, and follow study subjects for Phase I, II, III, and IV clinical trials, ensuring protocol compliance and close monitoring while the subjects are in study.
- Prepare study charts, binders, and supplies for offsite storage in conjunction with the Regulatory Specialist, when applicable.
- Inform and document notification of the subject’s Primary Care Physician of trial participation if approved by the subject.
- Ensure duplication of each for filing in the subject source and with the regulatory specialist.
- Report all Serious Adverse Events to the principal investigator, sponsor, and IRB as outlined in the protocol and site SOP. If need be, contact the subject’s primary care physician or specialist.
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