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, entry, quality assurance, and compliance while collaborating with research teams in a remote work environment.

Key responsibilities

• Enter and manage clinical trial data in EMR, CTMS, and EDC systems while ensuring data accuracy and compliance
• Collaborate with sponsors and clinical teams to resolve protocol issues and maintain regulatory compliance
• Support monitoring visits and audits, contributing to data management improvements and mentoring peers

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