Clinical Research Coordinator 1 - Olol

FMOLHS

Baton Rouge, LA, United States
Gcp guidelines
Fda regulations
Participant recruitment
The Clinical Research Coordinator I (CRC I) is responsible for assisting with the day-to-day activities of clinical research studies under the supervision of the Principal Investigator (PI) or Clinical Research Nurse and in accordance with Good Clinical Practice (GCP) guidelines, FDA regulations, and institutional policies

Job Summary

  • The Clinical Research Coordinator I (CRC I) is responsible for assisting with the day-to-day activities of clinical research studies under the supervision of the Principal Investigator (PI) or Clinical Research Nurse and in accordance with Good Clinical Practice (GCP) guidelines, FDA regulations, and institutional policies.
  • The CRC I is responsible for assisting with study operations, participant recruitment, and data management contributing to the overall success of clinical trials.
  • Our Lady of the Lake Health provides care for a full range of illness or injury, including those that are extremely complex, for both pediatric and adult patients.

Matching Summary

The Clinical Research Coordinator I (CRC I) is responsible for assisting with the day-to-day activities of clinical research studies under the supervision of the Principal Investigator (PI) or Clinical Research Nurse and in accordance with Good Clinical Practice (GCP) guidelines, FDA regulations, and institutional policies.

Skills & Requirements

Must-have

  • GCP guidelines
  • FDA regulations
  • participant recruitment
  • data management
  • informed consent
  • biological sample processing

Nice-to-have

  • excellent communication skills
  • business writing proficiency
  • planning and organization skills
  • attention to detail
  • Microsoft efficient

Key Requirements

  • Bachelor’s Degree in a related field
  • BLS certification

Work Rights

Not specified

Tailored Resume

Cover Letter