Research Coordinator in Stark Canton, Ohio at Gabrail Cancer Center Research
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Job Description
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:Key Responsibilities
- Study Coordination & Execution
o 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
o Screen and enroll study participants
o Conduct and support subject visits, including follow-up and retention activities
o Maintain study supplies, equipment, and inventory
o Maintain thorough knowledge of assigned protocols, investigational products, and study requirements
- Clinical & Data Responsibilities
o Perform clinical procedures as trained and delegated, including vital signs, ECGs, phlebotomy, and basic laboratory processing
o Accurately document study activities in source documents and electronic systems following ALCOA+ principles
o Resolve queries in a timely manner
- Regulatory & Quality Compliance
o Maintain complete, accurate, and inspection-ready source documentation
o Support quality management and the data department to prepare for and participate in monitoring visits, audits, and regulatory inspections
o Complete required trainings, certifications, and study documentation timely
o Escalate protocol deviations, noncompliance, or quality concerns promptly
- Collaboration & Communication
o Maintain professional, timely communication with investigators, sponsors, CROs, monitors, and Gabrail Cancer & Research Center/PhaseWell team members
o Support site initiation visits, and study-related training sessions
Qualifications
- Education & Experience
o At least one of the following is required:
§ Medical Assistant, LPN/LVN, EMT, or similar clinical credential
- Skills & Competencies
o Working knowledge of GCP, FDA regulations, and clinical research operations
o Strong organizational skills with high attention to detail
o Excellent written, verbal, and interpersonal communication skills
o Ability to manage multiple tasks and adapt to changing priorities
o Proficiency with CTMS, EHRs, and Microsoft Office/Teams
o Ability to handle sensitive information with professionalism, and in compliance with HIPAA