Senior Director, Compliance, Europe

Revolution Medicines is a clinical-stage precision oncology company focused on developing novel targeted therapies to inhibit frontier targets in RAS-addicted cancers. The companys 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.

The Opportunity:

RevMed is seeking an experienced compliance leader in Europe. As a key member of the Legal and Compliance function this is an excellent opportunity to lead a team and support the launch of new RevMed therapies and the Companys rapid business growth in Europe. 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 Companys operations.

Key Responsibilities:

Lead continuous development of Healthcare Compliance Programs in Europe in line with RevMeds global compliance strategy the Office of Inspector General (OIG) Compliance Program Guidance for Pharmaceutical Manufactures (OIG Guidance) applicable industry codes and best practices.

• Represent Compliance as the Compliance lead on the European Leadership team.

• Collaborate with cross-regions and implement global compliance initiatives in Europe.

• Provide compliance leadership and oversight for review and approval processes for core Commercial and Medical activities: grants sponsorships speaker bureau advisory boards and other initiatives involving interactions with healthcare professionals healthcare organizations governments and patient advocacy groups.

• Provide healthcare compliance subject matter expertise in the development of appropriate systems tools and technology solutions to enhance the efficiency and effectiveness of the Healthcare Compliance Program relating to common HCP interactions such as advisory boards consulting engagements speaker programs sponsorships and grants.

• Establish and chair the Compliance Committee in Europe; provide regular compliance related reports and other communications for multiple audiences in the Company including the Compliance Committee Commercial Leadership Medical Affairs teams and country management teams.

• Collaborate with the Head of Compliance on the design and execution of internal reviews risk assessments monitoring and auditing to ensure that compliance policies and procedures function as intended and the Company identifies potential compliance risks and remediates where necessary.

• Support Head of Global Compliance in the conduct and resolution of compliance investigations as needed including the implementation of corrective and preventive actions plans.

• Proactively identify legal and regulatory issues industry trends industry codes and practices applicable to compliance.

• Partner with the Head of Global Compliance to build develop and manage the European compliance team including hiring onboarding performance management mentoring and establishing scalable operating models to support the Companys growth in Europe.

• Advise on the adoption of new or revision of existing policies and procedures to ensure compliance with laws regulations and applicable industry codes globally and regionally.

• Develop and monitor the execution of a comprehensive compliance training program for Europe employees and designated third parties on applicable compliance policies laws and regulations.

• Foster a culture of compliance and integrity in the region.

Required Skills Experience and Education:

• Minimum of 12 years relevant experience including in-house pharmaceutical experience developing compliance programs.

• Degree in Law required (LL.B. or equivalent).

• Experience managing people teams and dotted-line reports.

• Extensive experience with compliance matters relating to the development approval and commercialization of pharmaceutical products in Europe.

• Comprehensive knowledge of healthcare fraud and abuse laws and transparency requirements as well as industry codes in European countries.

• 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.

• 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.

• Fluent in English and at least one other language.

• Excellent organizational skills and problem-solving capabilities and the ability to perform in a fast-paced high volume deadline-driven environment.

• 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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