Clinical Research Coordinator, Freeman Lab

The University of Texas at Austin

Austin, TX, US
Base: $53,454; bonus/equity: not specified; benefi...
Fully remote
3 years clinical research experience
Ich-gcp and fda regulatory knowledge
Edc/ctms system proficiency
The Clinical Research Coordinator manages day-to-day study operations ensuring protocol fidelity, participant safety, and regulatory compliance

Job Summary

  • The Clinical Research Coordinator manages day-to-day study operations ensuring protocol fidelity, participant safety, and regulatory compliance.
  • Responsibilities include recruiting participants, obtaining informed consent, conducting study visits, and maintaining accurate source data in EDC systems.
  • The role requires deep expertise in ICH-GCP guidelines and the ability to collaborate with investigators, sponsors, and ancillary departments.

Matching Summary

The Clinical Research Coordinator manages day-to-day study operations ensuring protocol fidelity, participant safety, and regulatory compliance.

Salary

Base: $53,454; Bonus/Equity: Not specified; Benefits: Teacher Retirement System (TRS) eligible

Skills & Requirements

Must-have

  • 3 years clinical research experience
  • ICH-GCP and FDA regulatory knowledge
  • EDC/CTMS system proficiency
  • Participant screening and consent procedures
  • Source data verification and documentation

Nice-to-have

  • Oncology or neurology trial experience
  • Phlebotomy and ECG competencies
  • ACRP CCRC or SOCRA CCRP certification
  • Epic research module experience
  • Strong interpersonal communication skills

Key Requirements

  • Bachelor's degree in health or life science
  • 3 years of clinical research coordination experience
  • Current GCP training consistent with ICH-GCP E6
  • Eligibility for ACRP CCRC or SOCRA CCRP certification

Work Rights

Must have authorization to work in the United States

Tailored Resume

Cover Letter