Job Details

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