We are seeking a detail-oriented Clinical Research Regulatory & Source Document Specialist to support our growing clinical research team. This position is responsible for creating and maintaining source documents, reviewing protocol amendments, updating study materials, and ensuring research documentation remains accurate, organized, and compliant with sponsor and regulatory requirements.

The ideal candidate is highly organized, proactive, and experienced in clinical research documentation and protocol management.

Responsibilities

• Create, update, and maintain study source documents for clinical trials
• Review protocol amendments and identify required study changes
• Update source packets, visit worksheets, logs, and study tools following protocol revisions
• Ensure all study documents remain compliant with sponsor, GCP, and site requirements
• Communicate protocol and amendment changes to research...