Clinical Trials Regulatory Advisor

SLAC; Palo Alto (CA); On-site; USD 70,000 - 110,000; Full time

Job summary

Stanford Medicine's Department of Anesthesiology, Perioperative and Pain Medicine is seeking a Clinical Trials Regulatory Specialist 1 to provide centralized regulatory support for a diverse portfolio of clinical research.

The role covers study start-up, regulatory submissions, IRB navigation, staff training, SOP development, and compliance oversight to ensure timely approvals and high-quality submissions.

Responsibilities

• Prepare and submit regulatory packets for new studies.
• Provide regulatory guidance and training to investigators and staff.
• Coordinate regulatory update meetings and navigate IRB inquiries and submissions.
• Develop and maintain SOPs, quick-reference guides, and best-practice documents for regulatory practices.
• Support compliance and process improvements, and act as liaison for safety reporting and audits.

Job description

Stanford Medicine's Department of Anesthesiology, Perioperative and Pain Medicine is seeking a Clinical Trials Regulatory Specialist 1 to provide centralized regulatory support for a diverse portfolio of clinical research.

The role covers study start-up, regulatory submissions, IRB navigation, staff training, SOP development, and compliance oversight to ensure timely approvals and high-quality submissions.