Principal Clinical Research Associate

Job Summary

To enhance clinical monitoring standards, the full-time remote Principal Clinical Research Associate will own the monitoring rubric, teach team members through real work, and serve as the senior escalation point for complex monitoring issues while maintaining a small caseload of approximately 25-35%.

Key responsibilities

• Own and maintain a living rubric and library for monitoring standards and practices
• Teach team members by reviewing their monitoring work side-by-side against established standards
• Act as the senior escalation point for complex monitoring challenges and facilitate team independence over time

Required qualifications

• Extensive experience in clinical monitoring with a strong background in SDV/review and protocol compliance
• In-depth understanding of clinical guidelines such as GCP/ICH and risk-based monitoring
• Proven ability and desire to mentor and train other monitors effectively
• Strong writing skills for creating clear and precise documentation
• Ability to collaborate effectively in a remote work environment with required daily overlap with UTC+8