Clinical Research Coordinator Ii

Care Access

Springfield, United States
On-site
Good clinical practices (gcp)
Protocol timelines adherence
Fda regulations and ich guidelines
The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance

Job Summary

  • The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.
  • Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with clinical staff and Sponsor/CRO representatives.
  • Record data legibly and enter in real time on paper or e-source documents.

Matching Summary

The Clinical Research Coordinator’s primary responsibilities are to utilize Good Clinical Practices (GCP)s in the process of screening, enrolling and closely monitoring clinical research study subjects while ensuring protocol and regulatory compliance.

Skills & Requirements

Must-have

  • Good Clinical Practices (GCP)
  • protocol timelines adherence
  • FDA regulations and ICH guidelines
  • patient interaction
  • adverse event identification
  • informed consent process
  • data recording and entry
  • study medication management

Nice-to-have

  • positive professional manner
  • effective relationships with personnel
  • assist with recruitment materials

Key Requirements

  • GCP knowledge
  • FDA regulations knowledge
  • ICH guidelines knowledge
  • Basic clinical procedures training

Work Rights

Not specified

Tailored Resume

Cover Letter