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Clinical Research Coordinator

  • Clinical Research Coordinator job type Posted on: Nov 05, 2026
  • Clinical Research Coordinator experience level PRIME CLINICAL RESEARCH INC
  • Clinical Research Coordinator employment type Lewisville, Texas
  • Clinical Research Coordinator employment type Onsite
  • Clinical Research Coordinator salary Full-time
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Job Title :

Clinical Research Coordinator

Job Type :

Full-Time

Job Location :

Lewisville Texas United States

Remote :

No

Jobcon Logo Job Description :

View Full Description

Job Description

Job Description
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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Jobcon Logo Position Details

Posted:

Nov 05, 2026

Reference Number:

b1ff3f051

Employment:

Full-time

City:

Lewisville

Job Origin:

ziprecruiter

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Job Description

Job Description
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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