Clinical Research Coordinator without Regulatory

Study Coordinator – Clinical Research (Clinical Operations) Prime Clinical Research Location: On-Site Employment Type: Full-Time Department: Clinical Operations Prime Clinical Research is seeking a Study Coordinator 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 2 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 #J-18808-Ljbffr HR Anew