What are the responsibilities and job description for the Clinical Research Coordinator position at Prime Clinical Research Inc?
Benefits:
Prime Clinical Research Inc is looking for a dedicated and detail-oriented Clinical Research Coordinator to join our growing team in Mansfield, TX. This is an exciting opportunity to play a key role in advancing medical research and making a real difference in patients' lives. If you're passionate about clinical trials and thrive in a fast-paced, science-driven environment, we want to hear from you!
Responsibilities:
Prime Clinical Research Inc is a dedicated clinical research organization based in Mansfield, TX, committed to advancing healthcare through rigorous and ethical clinical trials. Our team is passionate about connecting patients with innovative treatment options while maintaining the highest standards of safety and scientific integrity. We foster a collaborative, mission-driven workplace where every team member's contributions directly impact the future of medicine.
- 401(k)
- Employee discounts
- Health insurance
- Paid time off
Prime Clinical Research Inc is looking for a dedicated and detail-oriented Clinical Research Coordinator to join our growing team in Mansfield, TX. This is an exciting opportunity to play a key role in advancing medical research and making a real difference in patients' lives. If you're passionate about clinical trials and thrive in a fast-paced, science-driven environment, 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 a primary point of contact for study sponsors, IRBs, and clinical monitors
- Prepare and submit regulatory documents, including IRB submissions and protocol amendments
- Administer study procedures, collect biological samples, and perform assessments per protocol
- Ensure participant safety and informed consent compliance throughout all study phases
- Bachelor's degree in a health science, biology, or related field preferred
- Prior experience in clinical research coordination or a clinical setting strongly preferred
- Knowledge of GCP, FDA regulations, and IRB submission processes
- ACRP or SOCRA certification (CCRC, CCRP) is a plus
- Strong attention to detail with excellent organizational and time management skills
- Proficiency with electronic data capture (EDC) systems and MS Office
- Excellent interpersonal and communication skills with a patient-centered approach
Prime Clinical Research Inc is a dedicated clinical research organization based in Mansfield, TX, committed to advancing healthcare through rigorous and ethical clinical trials. Our team is passionate about connecting patients with innovative treatment options while maintaining the highest standards of safety and scientific integrity. We foster a collaborative, mission-driven workplace where every team member's contributions directly impact the future of medicine.