Senior Clinical Trials Data Coordinator

A company is looking for a Sr Clinical Trials Data Coordinator. Key Responsibilities Coordinate data collection, entry, quality assurance, and query resolution for oncology clinical trials Ensure data accuracy and compliance with regulatory guidelines while managing adverse event documentation Support monitoring visits and contribute to data management improvements and training of research data staff Required Qualifications Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience 5-7 years of clinical research or related experience Completion of Good Clinical Practice (GCP) and Human Subjects Protection (HSP) training within 1 month of employment Ability to obtain SOCRA or ACRP certification within 2 years of employment Experience with Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR)