Director, Compliance, Italy

Revolution Medicines; Lombardia; On-site; EUR 150,000 - 210,000; Full time

Job summary

Revolution Medicines seeks an experienced compliance leader in Italy to design and drive the Healthcare Compliance Program across Italy. You will work with senior Commercial, Medical, Legal, Finance and HR leaders to implement Italian controls and policies, enabling launches and ongoing operations.

You will bring 10+ years of in‑house pharma compliance experience, strong stakeholder management, and deep knowledge of EU and Italian laws.

Qualifications

• 10 years’ relevant experience, including in‑house pharmaceutical experience developing compliance programs.
• Experience managing diverse stakeholders without direct reports.
• Experience with compliance in development, approval and commercialization of pharma products in Europe.
• Comprehensive knowledge of Italian anti‑corruption and healthcare compliance laws, including Legislative Decree 231/2001, Law 190/2012, the Sunshine Act, AIFA rules, Farmindustria Code of Conduct, and Decree 24/2023 on whistleblowing.
• Ability to apply a risk‑based analysis to compliance issues and develop compliant solutions.
• Strong written and verbal communication, professionalism.

Responsibilities

• Lead the continuous development of the Healthcare Compliance Program in Italy in line with RevMed’s global compliance strategy.
• Represent Compliance on the Italian Leadership team and advise local Commercial and Medical teams.
• Collaborate across functions to adapt global compliance initiatives in Italy.
• Oversee reviews of interactions with HCPs, HCOs, patient organizations, payors and officials.
• Monitor regulatory developments in Italy and advise on operational impact.
• Draft and implement compliance policies and training programs for Italy.
• Foster a culture of compliance and integrity throughout the Italian organization.
• Develop systems and tools to improve program efficiency and effectiveness.
• Design risk assessments, monitoring and audit plans for Italy and lead remediation.

Skills

Healthcare compliance

Regulatory compliance

Stakeholder management

Communication skills

Policy drafting

Training programs

Investigations

Risk assessment

Whistleblowing

European pharma experience

Job description

Revolution Medicines is a global, commercial‑state oncology company dedicated to discovering, developing and delivering innovative medicines for patients with RAS‑addicted cancers. Leveraging its differentiated RAS(ON) tri‑complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer‑driving state of RAS. Founded on rigorous scientific inquiry and a willingness to challenge long‑held assumptions, Revolution Medicines is committed to changing the trajectory of disease for patients with RAS‑addicted cancers worldwide.

Our people are united by a shared way of working: follow the science, challenge assumptions, act with urgency and hold ourselves to a high standard of rigor—all in service of patients.

The Opportunity:

RevMed is seeking an experienced compliance leader in Italy. As a key member of the Legal and Compliance function, this is an excellent leadership opportunity to enable the launch of new RevMed therapies and the Company’s rapid business growth in Italy. The position will contribute to the development and implementation of organizational strategies, policies and practices, and work with senior Commercial, Medical, Clinical Development, Legal, Finance and HR leadership to integrate appropriate healthcare, corporate and other compliance controls to guide the Company’s operations.

Experience:

An experienced compliance professional, ideally with a legal qualification. You are likely to have 10+ years’ experience in‑house pharmaceutical experience and a strong track record of setting up and leading a local or regional healthcare compliance framework. You must be able to demonstrate strong experience across all compliance pillars and be a strong communicator and team player.

Key responsibilities of this role include the following:

• Program Development and Strategic Alignment: Lead the continuous development of the Healthcare Compliance Program in Italy in line with RevMed’s global compliance strategy. Ensure the program is consistent with the values and principles of the organization and fit for purpose and complies with applicable Italian laws, regulations and industry codes.
• Local Business Advisory: Represent Compliance on the Italian Leadership team and serve as the primary compliance advisor to the local Commercial and Medical teams, providing risk‑based guidance across the product life cycle to enable successful launches and commercialization.
• Cross‑Functional Collaboration: Collaborate across functions and regions to adapt and implement global compliance initiatives in Italy.
• Activity Review and Certification: Provide compliance oversight of the review and approval of interactions with HCPs, HCOs, patient organizations, payors and government officials (including grants, sponsorships, speaker programs and advisory boards), and of the certification of promotional and non‑promotional materials and meetings.
• Regulatory & Code Monitoring: Proactively monitor and interpret legal, regulatory and industry‑code developments in Italy and advise the business on their operational impact.
• Policies and Procedures: Draft, implement and update compliance policies, procedures and guidance to ensure compliance with applicable laws, regulations and industry codes in Italy.
• Training: Develop, deliver and monitor a comprehensive compliance training program for employees in Italy, including field‑based personnel, and designated third parties.
• Compliance Culture: Foster a strong culture of compliance and integrity across the Italian organization.
• Systems and Process Innovation: Provide healthcare compliance subject matter expertise in developing compliance systems, tools and technology solutions that improve the efficiency and effectiveness of the program for common HCP interactions.
• Monitoring, Auditing and Risk Assessment: Design and execute the risk assessment, monitoring and auditing plan for Italy, and lead remediation where necessary.
• Investigations and Speak‑Up: Administer local whistleblowing channels and support in compliance investigations, including corrective and preventive action plans.
• Third‑Party Risk Management: Own risk‑based due diligence and ongoing monitoring of third parties (distributors, agencies, consultants and vendors) under applicable anti‑corruption and transparency requirements.
• Reporting and Transparency: Support the Compliance Committee and transparency reporting obligations, and provide regular compliance reports to the Compliance Committee, Commercial Leadership, Medical Affairs and country management.
• Stakeholder Liaison: Act as compliance liaison with AIFA, Farmindustria and other Italian authorities and industry associations, managing responses to code complaints, inquiries and investigations.

Required Skills, Experience and Education:

• 10 years’ relevant experience, including in‑house pharmaceutical experience developing compliance programs.
• Demonstrated track record of working successfully as an individual contributor while managing a wide range of stakeholders and client groups, 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 a risk‑based analysis to compliance issues and demonstrate creativity and flexibility in developing solutions that satisfy both business requirements and legal obligations.
• Strong critical thinking skills, attention to detail, adaptability, communication skills and professionalism.
• Ability to work in a matrix organization, collaborate with business partners, influence peers and interact with both senior management and Field Force, Medical and Market Access teams.
• Ability to manage and serve a wide range of client groups by recognizing and responding quickly and pragmatically to urgent situations.
• Exceptional and demonstrated written and verbal communication skills and interpersonal skills in both one‑on‑one and group settings, as well as proven negotiation skills.
• Excellent organizational skills and problem‑solving capabilities and the ability to perform in a fast‑paced, high volume, deadline‑driven environment.
• Confidence to advise stakeholders at all levels.
• Appropriate judgment to liaise with Legal and business colleagues and/or outside counsel as needed.
• Commitment to being a team player with the desire to be helpful in other areas covered by a growing Compliance department.

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