Clinical Research Protocol Specialist

Job Summary

To support the Precision Oncology Program within the Department of Veterans Affairs, the full-time Clinical Research Protocol Specialist will develop, coordinate, and manage clinical trial protocols while working remotely and collaborating with physician-scientists and research leadership.

Key responsibilities

• Collaborate with stakeholders to develop clinical trial and research protocols from initial concept through final submission
• Draft and manage protocol documents, informed consent forms, and regulatory submissions
• Coordinate protocol development activities and support compliance with regulatory standards across multiple studies

Required qualifications

• Bachelor's degree in Life Sciences, Public Health, Clinical Research, or a related field
• Minimum of eight years of experience in clinical research, protocol development, or regulatory affairs
• Demonstrated experience in writing and coordinating clinical trial protocols
• Working knowledge of Good Clinical Practice (GCP) and human subjects research regulations
• Ability to obtain and maintain a Public Trust clearance