Biology, Certified Clinical Research Coordinator (CCRC), Clinical Data Collection, Clinical Research, Clinical Study Publications, Clinical Support, Clinical Trial, Clinical Trial Management, Data Entry, Data Management, Documentation, Electronic Data Capture (EDC), GCP (Good Clinical Practices), ICH Regulations, Informed Consent, Operational Support, Organizational Skills, Pediatrics, Phlebotomy, Public Health, Record Keeping, Regulations, Research Protocols, Sample/Specimen Processing, Specimen Collection
Clinical Research Coordinator (without Regulatory)
Prime Clinical Research
Location: On-Site
Employment Type: Full-Time
Department: Clinical Operations
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.
What You Will Do
Clinical Trial Coordination
- 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
Visit Preparation and Execution
- Prepare charts, documentation, and study materials prior to visits
- Ensure protocol-required procedures and assessments are completed
Clinical Support
- Perform or assist with specimen collection including blood draws
- Process and document samples according to study protocol
Data Management
- Enter study data into Electronic Data Capture (EDC) systems
- Maintain accurate source documentation
- Respond to sponsor data queries and maintain organized study records
Study Operations
- Track participant visits and follow-up schedules
- Support monitoring visits and sponsor requests
Qualifications
Required
- 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
Preferred
- Clinical research certification (CCRC or CCRP)
- Experience coordinating multiple clinical research studies
- Experience working with pediatric populations
Compensation
Salary Range: $45,000 – $55,000 depending on experience