Senior Manager, Clinical Business Systems

<p>Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers.  The company’s R&D pipeline comprises RAS(ON) Inhibitors designed to suppress diverse oncogenic variants of RAS proteins, and RAS Companion Inhibitors for use in combination treatment strategies. As a new member of the Revolution Medicines team, you will join other outstanding Revolutionaries in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway.</p> <p><strong>The Opportunity:</strong></p> <p>The Senior Manager, Clinical Systems is a hands-on technical leader responsible for the daily administration, support, and ongoing enhancement of core clinical systems, including eTMF and CTMS, as well as the implementation and optimization of future platforms that support clinical operations (e.g., RBQM, Study Start-Up, IRT/RTSM).</p> <p>This role will actively perform and oversee system configuration, user management, periodic reviews, and validation activities, ensuring systems remain compliant, reliable, and inspection ready. The individual will work closely with Clinical Operations, Data Management, Regulatory, CSV, Quality, and external vendors to support business needs while maintaining GxP compliance. Key responsibilities in this role include:</p> <ul> <li> <p>Act as the hands-on system owner/lead for assigned clinical systems, supporting daily operations and issue resolution.</p> </li> <li> <p>Perform user lifecycle management activities including provisioning, modifications, deactivation, and role-based access control.</p> </li> <li> <p>Execute and document periodic user access reviews and audit trail reviews in alignment with SOPs and regulatory requirements.</p> </li> <li> <p>Perform system configuration updates, including role updates, metadata changes, and system enhancements.</p> </li> <li> <p>Support and participate in system implementations, upgrades, and integrations, including hands-on validation activities.</p> </li> <li> <p>Execute release management activities, including impact assessments, regression testing, and coordination of deployments.</p> </li> <li> <p>Manage and execute change control activities, including documentation, risk assessment, and approvals.</p> </li> <li> <p>Troubleshoot system issues, coordinate with vendors, and track resolution through ticketing systems (e.g., ServiceNow).</p> </li> <li> <p>Generate and review system reports to support compliance, audit readiness, and operational oversight.</p> </li> <li> <p>Ensure systems operate in compliance with 21 CFR Part 11, EU Annex 11, GAMP 5, and ALCOA+ data integrity principles.</p> </li> <li> <p>Support internal audits and health authority inspections by providing documentation, reports, and system walkthroughs.</p> </li> <li> <p>Partner with cross-functional teams to support end-user training, adoption, and process improvements.</p> </li> </ul> <p><strong>Required Skills, Experience and Education:</strong></p> <ul> <li> <p>Bachelor's degree in information systems, Computer Science, Life Sciences, or related field.</p> </li> <li> <p>5- 7 years of hands-on experience supporting clinical or GxP-regulated systems in a biotech or pharmaceutical environment.</p> </li> <li> <p>Veeva Vault administrator certification is strongly preferred.</p> </li> <li> <p>Strong experience with system administration, user access management, and periodic reviews.</p> </li> <li> <p>Hands-on experience supporting validated SaaS platforms and system implementations.</p> </li> <li> <p>Experience executing validation deliverables.</p> </li> <li> <p>Strong understanding of change control, release management, and system lifecycle processes.</p> </li> <li> <p>Working knowledge of 21 CFR Part 11, EU Annex 11, GAMP 5, and risk-based validation approaches.</p> </li> <li> <p>Ability to troubleshoot issues and translate business needs into system configurations.</p> </li> <li> <p>Strong documentation and communication skills.</p> </li> </ul> <p><strong>Preferred Skills:</strong></p> <ul> <li> <p>Hands-on experience with Transperfect Trial Interactive eTMF and eClinical Elluminate platfoms</p> </li> <li> <p>Experience with audit trail review, role-based security models, and inspection readiness.</p> </li> <li> <p>Familiarity with identity and access management tools (e.g., Active Directory, Azure Entra).</p> </li> <li> <p>Experience with ServiceNow or similar ticketing systems.</p> </li> <li> <p>Exposure to clinical data standards and regulatory submission processes. </p> <p class="p1"><span style="color: rgb(255, 255, 255);">#LI-Hybrid  #LI-YG1</span></p> </li> </ul><div class="content-pay-transparency"><div class="pay-input"><div class="description"><p>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.</p> <p>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.</p> <p>Revolution Medicines is an equal opportunity employer and prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital status, medical condition, and veteran status.</p> <p>Revolution Medicines takes protection and security of personal data very seriously and respects your right to privacy while using our website and when contacting us by email or phone. We will only collect, process and use any personal data that you provide to us in accordance with our <a href="https://www.revmed.com/ccpa-notice">CCPA Notice</a> and <a href="https://www.revmed.com/privacy-policy">Privacy Policy</a>. For additional information, please contact <a href="mailto:privacy@revmed.com">privacy@revmed.com</a>.</p></div><div class="title">Base Pay Salary Range</div><div class="pay-range"><span>$164,000</span><span class="divider">—</span><span>$205,000 USD</span></div></div></div><div class="content-conclusion"><hr> <p><em>We are aware of recent recruitment scams in which individuals or organizations falsely represent themselves as being affiliated with Revolution Medicines. These scams may appear as false job advertisements or unsolicited contacts through communication or chat platforms, email, phone, or text message.</em><br><em> </em><br><em>Please note that Revolution Medicines does not extend unsolicited employment offers and will never ask candidates to provide financial information, purchase equipment, or pay fees as part of the hiring process. All legitimate communication from Revolution Medicines will come from an official <strong>@revmed.com</strong> email address.</em><br><em> </em><br><em>If you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to <span style="color: rgb(35, 111, 161);"><strong>careers@revmed.com</strong></span> so we can share these impersonations with our IT team for tracking and awareness.</em></p> <hr> <p> </p></div>