Clinical Research Coordinator

Job Summary

To support the clinical team, the full-time Clinical Research Source Development Coordinator will manage the creation, maintenance, and control of source documents for clinical trials, ensuring compliance with GCP guidelines and relevant protocols while working remotely.

Key Responsibilities

• Create and update source documents in accordance with GCP Guidelines and 21 CFR Part 11 Compliance
• Coordinate the review and release process for source documents, maintaining version control and organization
• Communicate daily with site staff and internal departments to support ongoing clinical studies and maintain accurate documentation

Required Qualifications

• Associate's degree in technology, biological science, business, or related field, or equivalent combination of education and experience
• 1+ years of clinical research experience, with strong knowledge of clinical trials and source document design preferred
• Proficiency in Microsoft applications, electronic health records, and web applications
• Strong organizational skills and attention to detail
• Ability to handle sensitive information confidentially and professionally in compliance with HIPAA guidelines