Clinical Research Coordinator (Houston)
MedixHouston, TX, United Statesjob_description.job_card.variable_days_ago
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job_description.job_card.job_descriptionAssist 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 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 CCRC or ACRP certification must pass background check, health and drug screening to begin position
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 :
Requirements :
Preferred Qualifications :
Location : Houston, TX
Schedule : 40 hours a week.
Start Date : ASAP
Employment Type : Full-Time
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Clinical Research Coordinator • Houston, TX, United States