Job Details

A company is looking for a Sr Clinical Trials Data Coordinator.Key ResponsibilitiesCoordinate data collection, entry, quality assurance, and query resolution for oncology clinical trialsEnsure data accuracy and compliance with regulatory guidelines while managing adverse event documentationSupport monitoring visits and contribute to data management improvements and training of research data staffRequired QualificationsBachelor's degree in Science, Health, or a related field, or equivalent relevant work experience5-7 years of clinical research or related experienceCompletion of Good Clinical Practice (GCP) and Human Subjects Protection (HSP) training within 1 month of employmentAbility to obtain SOCRA or ACRP certification within 2 years of employmentExperience with Clinical Trial Management Systems (CTMS) and Electronic Medical Records (EMR)