Research Coordinator

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
• 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
• Clinical & Data Responsibilities
• 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
• Regulatory & Quality Compliance
• 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
• Collaboration & Communication
• 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
  
  

Qualifications

• Education & Experience
• At least one of the following is required:
• Medical Assistant, LPN/LVN, EMT, or similar clinical credential
• Skills & Competencies
• 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