Clinical Research Coordinator (without Regulatory)
HR Anew•Mansfield, TX
•$45,000 - $55,000•Onsite
About The Position
Prime Clinical Research is seeking a Clinical Research Coordinator (without Regulatory) experience to support the operational execution of clinical trials. This role focuses on participant coordination, visit preparation, specimen collection, and data documentation across active clinical studies. This position does not include regulatory documentation responsibilities and focuses on the operational coordination of clinical trial visits and participant management. Candidates with experience as a Clinical Research Coordinator (CRC) or Clinical Trials Coordinator are encouraged to apply.
Requirements
- Bachelor’s degree in life sciences, healthcare, public health, or related field, or equivalent clinical research experience
- Minimum 3 years of clinical research experience as a Study Coordinator, Clinical Research Coordinator (CRC), or similar role
- Knowledge of ICH-GCP guidelines
- Experience using Electronic Data Capture (EDC) systems
- Strong organizational and documentation skills
- Phlebotomy or specimen collection experience
Nice To Haves
- Clinical research certification (CCRC or CCRP)
- Experience coordinating multiple clinical research studies
- Experience working with pediatric populations
Responsibilities
- Screen potential research participants according to study eligibility criteria
- Coordinate and schedule participant visits including screening, baseline, and follow-up visits
- Guide participants through the informed consent process
- Prepare charts, documentation, and study materials prior to visits
- Ensure protocol-required procedures and assessments are completed
- Perform or assist with specimen collection including blood draws
- Process and document samples according to study protocol
- Enter study data into Electronic Data Capture (EDC) systems
- Maintain accurate source documentation
- Respond to sponsor data queries and maintain organized study records
- Track participant visits and follow-up schedules
- Support monitoring visits and sponsor requests
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
