California Licensed Clinical Trials Coordinator

Job Summary

Supporting complex oncology clinical trials, the full-time salaried Senior Clinical Trials Data Coordinator will manage data collection, ensure compliance with regulatory standards, and collaborate with research teams while working remotely.

Key responsibilities

• Enter and manage clinical trial data in EMR, CTMS, and EDC systems, ensuring accuracy and compliance throughout the study lifecycle
• Perform quality checks and resolve data discrepancies to maintain regulatory compliance with FDA, ICH-GCP, and HIPAA guidelines
• Collaborate with sponsors and clinical coordinators to support monitoring visits, audits, and continuous data management improvements

Required qualifications

• Bachelor's degree in Science, Health, or a related field, or equivalent relevant work experience
• Minimum of 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), Electronic Medical Records (EMR), and eRegulatory systems