Clinical Research Coordinator (Houston) Job at Medix, Houston, TX

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  • Medix
  • Houston, TX

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, Part time, Work at office, Immediate start,

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