Clinical Trials Assistant

JOB SUMMARY

Perform a variety of duties include coordinating aspects of clinical trial protocols including but not limited to study initiation, recruitment, study visits, monitor visits, regulatory compliance, and study close-out.

ESSENTIAL DUTIES/RESPONSIBILITIES

  • Act as a liaison between providers, study representatives and patients.
  • Maintain case report forms, source documents and regulatory documents.
  • Pack and ship patient labs and review lab results.
  • Provide patient care and collect medical information during visit.
  • Initiate and participate in the informed consent process.
  • Conduct screening of prospective study participants and schedule appointments of patients interested in research studies.
  • Instruct patients regarding study protocols.
  • Arrange for or perform phlebotomy.
  • Assist in formulating and actively participate in the subject recruiting process.
  • Perform related work as required.