Associate Director, Regulatory Operations at Revolution Medicines

Ideal for a Regulatory Operations professional with 8+ years of experience in the biopharmaceutical industry, particularly in publishing and regulatory submissi

Work type: hybrid

Location: Redwood City, California, United States

Salary: $186,000 – $233,000/yr

Type: Full-time

Summary

Ideal for a Regulatory Operations professional with 8+ years of experience in the biopharmaceutical industry, particularly in publishing and regulatory submissions, holding at least a Bachelor's degree in a life science or related field. **What makes it worth a look...** Revolution Medicines is offering a full-time Associate Director, Regulatory Operations role with a strong salary range of USD 186,000 - 233,000 per year, based in Redwood City, California, with a hybrid work arrangement. **You might be a good fit if you...** * Have expert-level proficiency with eCTD publishing tools, including Veeva Vault RIM. * Can manage and execute regulatory submission activities for global Health Authorities. * Possess a thorough understanding of eCTD publishing standards and guidelines.

Job Description

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.

The Opportunity:

The Associate Director, Regulatory Operations will serve as a key publishing lead within the Regulatory Operations function, responsible for managing and executing regulatory submission activities to support the company’s growing pipeline and portfolio. This individual will ensure timely, accurate, and compliant submissions to the FDA and other global Health Authorities while contributing to the effective management of regulatory information, systems, and processes that enable operational efficiency and scalability.

This role is an individual contributor with leadership responsibilities, partnering cross-functionally with clinical, quality, CMC, nonclinical, and regulatory strategy teams to ensure seamless document management, publishing, and submission execution. The Associate Director also plays a key role in maintaining the integrity of regulatory information and ensuring compliance with global health authority requirements in a dynamic, fast-paced environment.

Regulatory Publishing & Submission Management

• Oversee the planning, preparation, publishing, submission, and archiving of regulatory dossiers in eCTD format for multiple FDA applications and global submissions.

• Manage submission production and quality control (QC) processes, ensuring compliance with global regulatory requirements and internal standards.

• Provide technical expertise in eCTD publishing tools and platforms (e.g., Veeva Vault RIM) to enable efficient and compliant submission execution.

• Proactively manage publishing timelines from request through archive, anticipating potential issues, escalating risks early, and collaborating with cross-functional teams to adapt plans as needed.

• Support the implementation, optimization, and maintenance of regulatory systems, tools, and technologies to improve submission efficiency and scalability.

• Partner with cross-functional stakeholders to ensure regulatory systems and workflows are well-documented, scalable, and aligned with business needs.

• Drive the development and continuous improvement of SOPs, templates, style guides, and document standards to support compliance and operational efficiency.

• Stay informed on emerging tools, technologies, and industry best practices, identifying opportunities to enhance submission operations and supporting the evaluation and adoption of innovative solutions where appropriate.

• Collaborate with internal stakeholders across clinical, CMC, quality, nonclinical, and regulatory strategy teams to coordinate the creation, review, and approval of regulatory submission documents.

• Manage relationships with publishing vendors and consultants, ensuring appropriate resource allocation and adherence to quality and delivery expectations.

• Provide training and guidance to internal teams on publishing procedures, tools, and best practices to ensure submission readiness.

• Communicate complex regulatory and operational issues clearly, providing solutions that balance compliance with the demands of growth and scale.

• Conduct gap analyses of regulatory operations policies, procedures, and SOPs, driving initiatives to enhance departmental efficiency and compliance.

• Maintain current knowledge of regulatory requirements, evolving eCTD guidance, and the broader regulatory operations landscape, providing interpretation and guidance to internal stakeholders.

• Bachelor’s degree in a life science, technical, or related field with 8+ years of Regulatory Operations and publishing experience in the biopharmaceutical industry; advanced degree preferred.

• Expert-level proficiency in Microsoft Word, Adobe Acrobat Professional, Toolbox, and StartingPoint.

• Thorough understanding of eCTD publishing standards, submission formatting, transmission, and archiving regulations and guidelines.

• Experience preparing and submitting regulatory dossiers to multiple global Health Authorities; oncology experience is a plus.

• Demonstrated ability to manage and prioritize multiple FDA applications and submissions with overlapping deadlines while maintaining accuracy and compliance.

• Ability to anticipate risks and proactively identify solutions to potential publishing and submission challenges.

• Strong organizational skills with high attention to detail and the ability to work independently in a dynamic, fast-paced environment.

• Proven success collaborating with cross-functional teams and external vendors to deliver high-quality, compliant submissions.

• Excellent interpersonal and communication (written and verbal) skills; able to work effectively across multiple groups, maintaining professionalism, diplomacy, and a positive approach.

• Some experience with people management, such as mentoring, training, or overseeing vendors and consultants.

• Proficiency with Veeva Vault RIM or similar regulatory information management systems.

• Experience using Smartsheet or equivalent project management tools.

The base pay salary range for this full-time position for candidates working onsite at our headquarters in Redwood City, CA is listed below. The range displayed on each job posting is intended to be the base pay salary range for an individual working onsite in Redwood City and will be adjusted for the local market a candidate is based in. Our base pay salary ranges are determined by role, level, and location. Individual base pay salary is determined by multiple factors, including job-related skills, experience, market dynamics, and relevant education or training.

Please note that base pay salary range is one part of the overall total rewards program at RevMed, which includes competitive cash compensation, robust equity awards, strong benefits, and significant learning and development opportunities.

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