Research Coordinator
About The Position
Position Overview Gabrail Cancer & Research Center, a PhaseWell Research site based in Canton, OH, is seeking a detail-oriented and patient-focused Clinical Research Coordinator (CRC) to support the execution of oncology clinical trials. With over 30 years of experience conducting Phase I–III clinical trials, Gabrail Cancer & Research Center has built a strong reputation for high-quality trial execution in oncology and hematology studies. The CRC is responsible for the day-to-day coordination of assigned clinical studies, ensuring participant safety, high-quality source documentation, and clinical functions. This role is ideal for a clinical research professional who thrives in a fast-paced, highly regulated environment and is passionate about advancing innovative therapies
Requirements
- Medical Assistant, LPN/LVN, EMT, or similar clinical credential
- Working knowledge of GCP, FDA regulations, and clinical research operations
- Strong organizational skills with high attention to detail
- Excellent written, verbal, and interpersonal communication skills
- Ability to manage multiple tasks and adapt to changing priorities
- Proficiency with CTMS, EHRs, and Microsoft Office/Teams
- Ability to handle sensitive information with professionalism, and in compliance with HIPAA
Responsibilities
- Coordinate and conduct primarily patient-facing and related study activities from site initiation through study close-out in accordance with protocol, GCP/ICH guidelines, FDA regulations, IRB requirements, and company SOPs
- Screen and enroll study participants
- Conduct and support subject visits, including follow-up and retention activities
- Maintain study supplies, equipment, and inventory
- Maintain thorough knowledge of assigned protocols, investigational products, and study requirements
- Perform clinical procedures as trained and delegated, including vital signs, ECGs, phlebotomy, and basic laboratory processing
- Accurately document study activities in source documents and electronic systems following ALCOA+ principles
- Resolve queries in a timely manner
- Maintain complete, accurate, and inspection-ready source documentation
- Support quality management and the data department to prepare for and participate in monitoring visits, audits, and regulatory inspections
- Complete required trainings, certifications, and study documentation timely
- Escalate protocol deviations, noncompliance, or quality concerns promptly
- Maintain professional, timely communication with investigators, sponsors, CROs, monitors, and Gabrail Cancer & Research Center/PhaseWell team members
- Support site initiation visits, and study-related training sessions
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree
