Jobs · Analyst · Texas

Clinical Research Coordinator

Prime Clinical Research Inc · Lewisville, TX · 2 wk ago
On-siteAnalystFull-time

Benefits

  • 401(k)
  • Employee discounts
  • Health insurance
  • Paid time off

About the Role

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!

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

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

About Us

Prime Clinical Research Inc. is a trusted clinical research site based in Lewisville, TX, committed to conducting high-quality trials that bring innovative treatments to patients. Our team is known for its dedication to participant safety, data integrity, and scientific excellence. We foster a collaborative and supportive work environment where every team member plays a vital role in advancing the future of medicine.

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