SQRL
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SQRL provided pay range
This range is provided by SQRL. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. About the Company Our client is a leading multi-phase, multi-therapeutic clinical research organization dedicated to advancing medical innovation through high-quality clinical trials. Their mission is to deliver excellence in patient care, regulatory compliance, and clinical data integrity across a network of research and standard-of-care sites. Each location operates state-of-the-art facilities staffed by experienced physicians, research professionals, and patient outreach teams. Overview
The Clinical Research Coordinator II or III is responsible for managing the day-to-day conduct of clinical trials under the direction of a Principal Investigator. This role involves protocol implementation, patient recruitment, data collection, and ensuring adherence to all regulatory and compliance standards. Key Responsibilities
Coordinate and implement assigned clinical research protocols in compliance with FDA regulations, GCP, and internal SOPs. Recruit, screen, and enroll study participants; ensure recruitment goals are achieved. Collect, record, and maintain accurate clinical data and source documentation. Prepare for and support study initiation, monitoring, and closeout visits. Manage investigational product accountability and maintain study supplies. Obtain informed consent and perform study procedures (phlebotomy, vitals, ECGs, lab processing, etc.). Monitor and document adverse events and serious adverse events per protocol. Maintain the clinical trial management system with real-time subject tracking and visit documentation. Assist with regulatory compliance, IRB submissions, and audit preparation. Train and mentor junior staff and serve as a liaison between investigators, site staff, and sponsors. Qualifications
Minimum 2 years of experience as a Clinical Research Coordinator (late-phase trials preferred). Associate’s or Bachelor’s degree in healthcare, life sciences, or related field (Master’s preferred). Strong understanding of GCP, ICH, and FDA regulatory standards. Excellent interpersonal, organizational, and data management skills. Proficiency with clinical trial management and EDC systems. GCP certification required; phlebotomy experience preferred. Competitive hourly pay Comprehensive health, dental, and vision insurance (HSA available with employer contribution) 401(k) with up to 6% employer match 3 weeks PTO + 5 days sick leave Short- and long-term disability Continuing education and tuition assistance Company-provided vehicle access for required travel Benefits
Medical insurance Vision insurance 401(k) Disability insurance Tuition assistance
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This range is provided by SQRL. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. About the Company Our client is a leading multi-phase, multi-therapeutic clinical research organization dedicated to advancing medical innovation through high-quality clinical trials. Their mission is to deliver excellence in patient care, regulatory compliance, and clinical data integrity across a network of research and standard-of-care sites. Each location operates state-of-the-art facilities staffed by experienced physicians, research professionals, and patient outreach teams. Overview
The Clinical Research Coordinator II or III is responsible for managing the day-to-day conduct of clinical trials under the direction of a Principal Investigator. This role involves protocol implementation, patient recruitment, data collection, and ensuring adherence to all regulatory and compliance standards. Key Responsibilities
Coordinate and implement assigned clinical research protocols in compliance with FDA regulations, GCP, and internal SOPs. Recruit, screen, and enroll study participants; ensure recruitment goals are achieved. Collect, record, and maintain accurate clinical data and source documentation. Prepare for and support study initiation, monitoring, and closeout visits. Manage investigational product accountability and maintain study supplies. Obtain informed consent and perform study procedures (phlebotomy, vitals, ECGs, lab processing, etc.). Monitor and document adverse events and serious adverse events per protocol. Maintain the clinical trial management system with real-time subject tracking and visit documentation. Assist with regulatory compliance, IRB submissions, and audit preparation. Train and mentor junior staff and serve as a liaison between investigators, site staff, and sponsors. Qualifications
Minimum 2 years of experience as a Clinical Research Coordinator (late-phase trials preferred). Associate’s or Bachelor’s degree in healthcare, life sciences, or related field (Master’s preferred). Strong understanding of GCP, ICH, and FDA regulatory standards. Excellent interpersonal, organizational, and data management skills. Proficiency with clinical trial management and EDC systems. GCP certification required; phlebotomy experience preferred. Competitive hourly pay Comprehensive health, dental, and vision insurance (HSA available with employer contribution) 401(k) with up to 6% employer match 3 weeks PTO + 5 days sick leave Short- and long-term disability Continuing education and tuition assistance Company-provided vehicle access for required travel Benefits
Medical insurance Vision insurance 401(k) Disability insurance Tuition assistance
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