Job Details

A company is looking for a Senior Clinical Trials Data Coordinator.Key ResponsibilitiesCoordinate data collection, entry, quality assurance, and query resolution for oncology clinical trialsEnsure regulatory compliance and data accuracy through quality checks and timely resolution of discrepanciesSupport monitoring visits, audits, and contribute to data management improvements and training of research staffRequired QualificationsBachelor's degree in Science, Health, or a related field, or equivalent relevant work experienceMinimum of 5-7 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), Electronic Medical Records (EMR), and eRegulatory systems