Clinical Research Coordinator

3 weeks ago


St Louis, United States Medix™ Full time

Experienced Clinical Research Coordinator (CRC)

The CRC is a member of the staff who wants to provide quality, compassionate care to patients while helping research promising new medicines. The CRC is self-motivated, highly organized, capable of managing multiple projects, and have at least two years of experience in the medical field.

Responsibilities

  • Perform overall data management of studies — collect, enter, and maintain records for clinical study subjects.
  • Support accurate and timely data entry in electronic databases.
  • Ensure all protocol-required procedures and visits occur according to specified guidelines.
  • Manage participant enrollment and ensure compliance with the protocol during participant recruitment, informed consent, participant education, eligibility assessment, participant care, and follow-up per protocol.
  • Collaborates with quality assurance (QA) in the development of source documentation for new studies, assisting in the assessment of toxicities/adverse events and reporting serious adverse events per IRB and sponsor requirements.
  • Possess excellent interpersonal skills and collaborative with the research team.
  • Independently manage workflows and prioritize numerous tasks.
  • Be flexible and anticipate time-frames to accommodate frames subjects, monitors, and overtime hours during high-enrolling study periods.
  • Maintains GCP certification and IATA training as required.
  • Performs other duties as assigned.


Requirements

  • At least two years of experience as a clinical research coordinator.
  • Excellent oral and written communication skills.
  • Demonstrated ability to work well independently and with subordinates.
  • Demonstrated ability to manage frequent deadlines and competing priorities.
  • Computer proficiency.
  • Critical thinking and analytical skills



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