California Licensed Clinical Trials Coordinator

Job Summary

A company is looking for a Senior Clinical Trials Data Coordinator.

Key Responsibilities

• Coordinate data collection, entry, quality assurance, and query resolution for oncology clinical trials
• Ensure data accuracy and regulatory compliance while managing adverse event documentation and study calendars
• Support monitoring visits, audits, 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), Electronic Medical Records (EMR), and eRegulatory systems