Medix™
This range is provided by Medix. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range
$25.00/yr - $35.00/yr Job Title: Clinical Research Coordinator
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. 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 Location:
Houston, TX Schedule:
40 hours a week. Start Date:
ASAP Employment Type:
Full-Time Seniority level:
Mid-Senior level Employment type:
Full-time Job function:
Research Industries:
Hospitals and Health Care Benefits: Medical insurance Vision insurance 401(k) Disability insurance
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$25.00/yr - $35.00/yr Job Title: Clinical Research Coordinator
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. 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 Location:
Houston, TX Schedule:
40 hours a week. Start Date:
ASAP Employment Type:
Full-Time Seniority level:
Mid-Senior level Employment type:
Full-time Job function:
Research Industries:
Hospitals and Health Care Benefits: Medical insurance Vision insurance 401(k) Disability insurance
#J-18808-Ljbffr