Clinical Research Coordinator
PRIME CLINICAL RESEARCH INC•Lewisville, TX
•Onsite
About The Position
Prime Clinical Research Inc. is looking for a dedicated and detail-oriented Clinical Research Coordinator to join our growing team in Lewisville, TX. This is an exciting opportunity to play a hands-on role in advancing medical research and improving patient outcomes. If you're passionate about clinical trials and making a real difference in healthcare, we want to hear from you!
Requirements
- Bachelor's degree in a health science, life science, or related field preferred
- 1+ years of experience in clinical research coordination or a related clinical setting
- Knowledge of FDA regulations, ICH-GCP guidelines, and IRB processes
- ACRP or SOCRA certification (CCRC, CCRP) is a plus
- Strong organizational skills with exceptional attention to detail
- Excellent communication and interpersonal skills for working with patients and sponsors
- Proficiency with electronic data capture (EDC) systems and MS Office
Nice To Haves
- ACRP or SOCRA certification (CCRC, CCRP)
Responsibilities
- Coordinate and manage day-to-day clinical trial operations in compliance with FDA regulations and GCP guidelines
- Screen, enroll, and monitor study participants throughout the duration of clinical trials
- Collect, record, and maintain accurate study data and source documentation
- Serve as the primary point of contact between sponsors, IRBs, and study participants
- Prepare and submit regulatory documents, including IRB submissions and protocol amendments
- Conduct informed consent processes and ensure participant safety and confidentiality
- Support site audits, monitor visits, and ensure protocol adherence
Benefits
- 401(k)
- Employee discounts
- Health insurance
- Paid time off
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
