Associate Director, Clinical Operations Enablement & Knowledge Systems

About the role

This is a unique opportunity for a Clinical Operations Professional who has innate leadership and organizational skills, technical expertise in clinical drug development in an industry setting and a drive to promote excellence. As an Associate Director (AD) Clinical Operations Enablement & Knowledge Systems, you will be a key member of the Clinical Operations Excellence team. You will be responsible for building and scaling the Clinical Operations "knowledge ecosystem"-including how information is structured, accessed, and applied-to enable consistent, efficient, and high-quality study execution across roles and programs. This is an execution-focused role that strengthens the capabilities of the Clinical Operations organization. The ideal candidate is a Clinical Operations leader who combines deep study execution experience with the ability to design scalable, user-centered systems that enable others to perform at their best. Lead the design and deployment of a scalable Clinical Operations knowledge ecosystem, including playbooks, toolkits and structured resources that enable consistent high quality study execution. Develop role-based enablement frameworks aligned to Clinical Operations responsibilities, study activities, and key transition points. Design and deliver multi-modal learning solutions (e.g., live sessions, on-demand modules, short-form videos, playbooks, and interactive resources) to maximize accessibility and adoption. Apply adult learning principles and user-centered design to ensure content is practical, engaging, and immediately applicable. Apply knowledge of Clinical Operations workflows and regulatory context (e.g., GCP, ICH) to ensure learning content is relevant, practical, and aligned with real-world study execution (this role does not own SOP development, GxP training, or inspection readiness activities). Support the successful onboarding of new Clinical Operations team members. Design and deliver targeted, "just-in-time" learning tools and experiences (e.g., checklists, quick guides, decision aids) to support critical activities and study milestones. Align learning and knowledge resources to key study lifecycle stages (e.g., study start-up, conduct, database lock, close-out). Define and implement a scalable structure for Clinical Operations knowledge, including how resources, tools, and guidance is organized, accessed, and maintained. Create intuitive, role-based pathways for accessing information across study lifecycle stages. Establish standards for maintaining and continuously improving operational knowledge. Own day-to-day planning, coordination, and delivery of learning activities, ensuring timeline, quality and outcomes are met. Track adoption, effectiveness and impact of learning and knowledge initiatives. Use feedback and performance insights to identify capability gaps and continuously improve tools, resources, and learning solutions. Evolve learning materials and resources to maintain alignment with Clinical Operations and cross-functional partner growth and needs. Partner with Clinical Operations and cross-functional team members to improve processes that will impact clinical trial management, quality and efficiency. Line management responsibilities including hiring, performance management, career development, and mentorship. This role does not own SOP authoring, GxP training delivery, or inspection readiness activities, but partners with relevant functions to ensure alignment. Participate in other Clinical Operations Excellence and Clinical Operations Activities as appropriate. Required Skills, Experience and Education: RN or Bachelor's degree in biological sciences or health-related field required. 11+ years direct Clinical Operations experience in the pharmaceutical or biotech industry, Relevant indirect experiences may also meet the requirement. Minimum of 5 years of line management experience. Strong working knowledge of FDA Regulations, ICH Guidelines, and GCP. Demonstrated experience successfully developing and authoring Clinical Operations and cross-functional handbooks, guidances or process templates in support of clinical operations or clinical study team management. Exper

Benefits

Additional Information

Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.

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