Job Description
Job Title: Clinical Research Coordinator
About the Role: (40 hrs week - fully onsite in Houston TX)
We are seeking a detail-oriented and motivated Clinical Research Coordinator (CRC) to join our client's Behavioral Health focused research team. The CRC will play a critical role in managing and coordinating clinical trials, ensuring compliance with Good Clinical Practice (GCP), sponsor protocols, and regulatory requirements.
- Phlebotomy skills required
- Strong behavioral health background (depression, addiction, PTSD)
- Must have experience specifically within Behavioral Health research
Key Responsibilities:
- Assist with study documentation and regulatory compliance
- Support data entry and maintenance in EDC systems
- Help schedule and track patient visits or study milestones
- Coordinate with study sponsors, investigators, and research staff
- Ensure accurate filing and organization of study documents
- Assist with IRB communications and submissions, if needed
Requirements:
- Previous experience in clinical research coordination
- Familiarity with regulatory requirements (GCP, IRB, FDA)
- Strong attention to detail and ability to manage tasks independently
- Excellent communication and organizational skills
- Proficient in using EDC systems, Microsoft Office, and email
Preferred Qualifications:
- CCRC or ACRP certification
*must pass background check, health and drug screening to begin position*
Location: Houston, TX
Schedule: 40 hours a week.
Start Date: ASAP
Employment Type: Full-Time
Job Tags
Full time, Immediate start, Work at office,