Senior Clinical Trials Data Coordinator

Job Summary

Supporting complex oncology clinical trials in a remote full-time capacity, the Senior Clinical Trials Data Coordinator will coordinate data collection, ensure quality assurance, and manage timely data entry into electronic data capture systems while collaborating closely with clinical teams and research staff.

Key responsibilities

• Coordinate data collection and quality assurance for oncology clinical trials, ensuring compliance with study requirements
• Review and resolve data discrepancies, maintaining accurate records and documentation in CTMS and EDC systems
• Participate in process improvement initiatives to enhance data management workflows and training materials

Required qualifications

• Bachelor's degree in Science, Health, or a related field from an accredited university, or equivalent working experience
• Minimum of 5-7 years of research or relevant experience
• Experience with Clinical Trial Management Systems (CTMS), Electronic Medical Records (EMR), and eRegulatory Systems
• SOCRA or ACRP Certification within 2 years of employment
• Preferably three years of oncology-specific research experience and proficiency in Excel