Revolution Medicines

Revolution Medicines

Associate Director, Global Healthcare Compliance Operations

Redwood City, California, United States · Director · Full-time

Sponsorship not specified$186k-$233kDetected 23 hours ago
Data AnalysisComplianceProject ManagementStakeholder ManagementAuditingProcess ImprovementProcurementFDA RegulatoryLeadershipCommunicationCollaborationProblem Solving

About the role

  • Assist the Director, Compliance with the development and execution of the global healthcare compliance operations strategy.
  • Identify opportunities to harmonize, streamline, and automate compliance-related workflows and systems.
  • Monitor operational performance and identify areas for process improvement and standardization.

Responsibilities

  • Expertise in process design, workflow optimization, and operational excellence.
  • Collaborative and influential cross-functional partner.
  • Establish and maintain scalable compliance processes and infrastructure to support the Company's global growth.
  • Develop operational metrics, dashboards, and key performance indicators to measure program effectiveness.
  • Partner with Compliance leadership to support continuous improvement initiatives and compliance program maturity.
  • Design and maintain operational processes supporting compliant HCP and HCO interactions globally.
  • Partner with IT, vendors, and business stakeholders to define requirements, prioritize enhancements, and manage system releases.
  • Ensure workflows appropriately support review, approval, documentation, contracting, payment, and record retention requirements.
  • Support development of controls and monitoring activities to ensure data integrity and reporting accuracy.
  • Develop and maintain compliance reporting and analytics capabilities.

Skills

  • Bachelor's degree required.
  • Advanced degree (MBA, JD, or equivalent) preferred.
  • Experience implementing and managing compliance-related systems and technology platforms.
  • Experience operating in a global pharmaceutical or biotechnology environment preferred.
  • Experience leading complex cross-functional projects and system implementations.
  • Strong project management and change management capabilities.
  • Experience with compliance technologies, workflow platforms, and reporting tools.
  • Excellent analytical, organizational, and stakeholder management skills.
  • Ability to translate compliance requirements into scalable business processes and technology solutions.
  • Strategic thinker with strong operational execution capabilities.

Compensation

  • $186,000 - $233,000 USD
  • 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.

Benefits

  • Collaborate with Medical Affairs, Commercial, Clinical, and Market Access stakeholders to implement efficient engagement processes.
  • Partner with Finance, Medical Affairs, and external vendors to ensure accurate data collection, reconciliation, validation, and reporting.

Company info

  • 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.

This listing is sourced directly from Revolution Medicines's careers page and normalized into a canonical job model.