Associate Director, Clinical Quality Assurance

Revolution Medicines is seeking an Associate Director, Clinical Quality Assurance, to provide leadership and compliance support for RevMed sponsored clinical trials with respect to RevMed’s Standard Operating Procedures, applicable regulatory requirements, and current industry standards and practices.

Requirements

• Bachelor’s degree in scientific or technical discipline
• A minimum of 10+ years of experience in GCP Quality in the pharmaceutical or biotechnology industry
• 8 years in any of the following areas: audit or audit management experience, inspection readiness, Deviation/CAPA management, or related quality management system responsibilities
• Extensive knowledge of ICH GCP, other relevant ICH guidelines and regulatory requirements (minimally US FDA) regarding applicable drug development regulations
• Effective communication (verbal and written)
• Ability to build and sustain positive relationships with GxP colleagues, internal stakeholders, and external partners
• Ability to create innovative solutions to problems, while integrating stakeholder input and feedback
• Ability to critically evaluate and troubleshoot complex problems with diligence
• Ability to manage multiple priorities and aggressive timelines
• Highly responsible, self-motivated professional with enthusiasm and passion for the work
• Highly proficient with various Microsoft and other computerized systems (e.g., Word, Outlook, Excel, PowerPoint, Visio, etc.)

Benefits

• Competitive cash compensation
• Robust equity awards
• Strong benefits
• Significant learning and development opportunities