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 complianceSupport data entry and maintenance in EDC systemsHelp schedule and track patient visits or study milestonesCoordinate with study sponsors, investigators, and research staffEnsure accurate filing and organization of study documentsAssist with IRB communications and submissions, if neededRequirements :
Previous experience in clinical research coordinationFamiliarity with regulatory requirements (GCP, IRB, FDA)Strong attention to detail and ability to manage tasks independentlyExcellent communication and organizational skillsProficient in using EDC systems, Microsoft Office, and emailPreferred Qualifications :
CCRC or ACRP certificationmust pass background check, health and drug screening to begin positionLocation : Houston, TX
Schedule : 40 hours a week.
Start Date : ASAP
Employment Type : Full-Time