Sr Clinical Trials Data Coord

About the role

The Senior Clinical Trials Data Coordinator supports complex oncology clinical trials from First-in-Human and Phase I through Phase IV by coordinating data collection, entry, quality assurance, and query resolution to ensure accurate, reliable, and compliant research data.

Responsibilities

• Interpret research protocols and review medical records to resolve discrepancies and maintain study visits and financial triggers within the Clinical Trial Management System (CTMS) aligned with Electronic Data Capture (EDC) systems.
• Work closely with physicians, clinical coordinators, and research teams to ensure timely data reporting, support adverse event data collection, and contribute to study monitoring and regulatory compliance.
• Perform peer data reviews, assist in the development of data management plans and workflows, and provide training and guidance to research data staff to maintain high-quality clinical trial data and efficient research operations.

Qualifications

• Minimum Education: Bachelor’s degree in Science, Health, or a related field from an accredited university, or equivalent relevant work experience.
• Minimum Experience: Minimum of 5–7 years of clinical research or related experience.
• Required Certifications: Completion of Good Clinical Practice (GCP) training within 1 month of employment. Completion of Human Subjects Protection (HSP) training within 1 month of employment. Ability to obtain SOCRA or ACRP certification within 2 years of employment.
• Systems Knowledge: Experience with Clinical Trial Management Systems (CTMS), Electronic Medical Records (EMR), and eRegulatory systems.