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Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Director Compliance

Regulatory Compliance & EthicsConfirmed live in the last 24 hours
Full-timeMilan, Metropolitan City of Milan, ItalyNo salary listedHybrid

About the Job

Requirements

  • At least 10 years of relevant experience, including in-house pharmaceutical experience developing compliance programs.
  • A demonstrated track record of working as an individual contributor while managing a wide range of stakeholders and client groups, and building compliance capabilities in a scaling organization without direct reports.
  • Extensive experience with compliance matters relating to the development, approval and commercialization of pharmaceutical products in Europe.
  • Comprehensive knowledge of Italian anti-corruption and healthcare compliance laws, including Legislative Decree 231/2001 (Organisational Model 231 and the Organismo di Vigilanza), Law 190/2012 on anti-corruption, the Sunshine Act (Law 62/2022) and its transparency and disclosure obligations, AIFA rules on promotion and scientific information under Legislative Decree 219/2006, the Farmindustria Code of Conduct, and Legislative Decree 24/2023 on whistleblowing.
  • Ability to apply risk-based analysis to compliance issues and develop solutions that satisfy business requirements and legal obligations.
  • Ability to work in a matrix organization, collaborate with business partners, influence peers, and interact with senior management and Field Force, Medical and Market Access teams.
  • Ability to manage and serve a wide range of client groups and respond quickly and pragmatically to urgent situations.
  • Written and verbal communication, interpersonal, and negotiation skills for one-on-one and group settings.
  • Organizational skills, problem-solving capabilities, and ability to perform in a fast-paced, high-volume, deadline-driven environment.
  • Confidence to advise stakeholders at all levels.
  • Judgment to liaise with Legal and business colleagues and/or outside counsel as needed.
  • Commitment to supporting other areas covered by a growing Compliance department.

Responsibilities

  • Lead the continuous development of the Healthcare Compliance Program in Italy in line with the company's global compliance strategy, ensuring alignment with organizational values and compliance with applicable Italian laws, regulations and industry codes.
  • Represent Compliance on the Italian Leadership team and serve as the primary compliance advisor to local Commercial and Medical teams, providing risk-based guidance across the product life cycle to support launches and commercialization.
  • Collaborate across functions and regions to adapt and implement global compliance initiatives in Italy.
  • Provide compliance oversight for review and approval of interactions with healthcare professionals, healthcare organizations, patient organizations, payors and government officials, including grants, sponsorships, speaker programs and advisory boards, and for certification of promotional and non-promotional materials and meetings.
  • Monitor and interpret legal, regulatory and industry-code developments in Italy and advise the business on their operational impact.
  • Draft, implement and update compliance policies, procedures and guidance to ensure compliance with applicable Italian laws, regulations and industry codes.
  • Develop, deliver and monitor a comprehensive compliance training program for employees in Italy, including field-based personnel, and designated third parties.
  • Foster a culture of compliance and integrity across the Italian organization.
  • Provide healthcare compliance expertise in developing compliance systems, tools and technology solutions to improve the efficiency and effectiveness of the program for common healthcare professional interactions.
  • Design and execute Italy's risk assessment, monitoring and auditing plan, and lead remediation where necessary.
  • Administer local whistleblowing channels and support compliance investigations, including corrective and preventive action plans.
  • Own risk-based due diligence and ongoing monitoring of third parties, including distributors, agencies, consultants and vendors, under applicable anti-corruption and transparency requirements.
  • Support the Compliance Committee and transparency reporting obligations, and provide regular compliance reports to the Compliance Committee, Commercial Leadership, Medical Affairs and country management.
  • Act as compliance liaison with AIFA, Farmindustria and other Italian authorities and industry associations, managing responses to code complaints, inquiries and investigations.

Desired Qualifications

  • An ideal candidate will have a legal qualification.

About the Company

Revolution Medicines

Clinical-stage oncology company developing RAS inhibitors

Revolution Medicines develops precision oncology drugs focused on cancers driven by RAS mutations. Its RAS(ON) inhibitors are small molecules that bind the active form of RAS to block cancer signaling, with candidates like Daraxonrasib (RMC-6236), Elironrasib (RMC-6291), and Zoldonrasib (RMC-9805) advancing in global Phase 3 trials. The company funds its research through collaborations, royalties, and upfront funding, and has not yet marketed a product. Its goal is to bring effective RAS-targeted therapies to patients and advance multiple candidates through late-stage trials toward approval, supported by strong cash reserves.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Redwood City, CA
Founded
2014

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