Clinical Research Coordinator 1 - OLOL

FMOLHS
Baton Rouge, LA
Category Research
Job Description
Assist with day-to-day activities of clinical research studies under the supervision of the Principal Investigator or Clinical Research Nurse, ensuring compliance with Good Clinical Practice guidelines and FDA regulations. Conduct study operations, participant recruitment, and data management, and contribute to the overall success of clinical trials.

Requirements

  • Assist in the coordination of clinical research studies
  • Ensure all study activities are conducted in compliance with the study protocol, GCP, and relevant regulatory guidelines
  • Screen, recruit, and enroll study participants according to the inclusion/exclusion criteria outlined in study protocols and as instructed by the PI
  • Obtain informed consent from study participants and ensure their understanding of study procedures
  • Conduct basic clinical assessments
  • Accurately collect, record, and maintain study data in case report forms or electronic systems
  • Collect and process biological samples, such as blood, urine, or tissue, following proper clinical and laboratory procedures
  • Monitor and report any adverse events, deviations, or protocol violations in a timely manner
  • Coordinate patient visits, follow-ups, and schedule necessary procedures and tests according to protocol
  • Ensure the safety of participants by following established safety protocols and guidelines
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