Study Coordinator Clinical Research Clinical Operations
HR Anew, Fort Worth, TX, United States
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
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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