ppRevolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company’s RD 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. /p h3The Opportunity: /h3 pWe are seeking a highly motivated and experienced professional to join our team as a Senior Director, Regulatory Affairs, Italy. Key aspects of this role will include leading and providing strategic input on all regulatory activities for assigned projects and territories in accordance with ICH requirements, Italian and EU regulations, and scientific and company policies and procedures. The role will work cross-functionally with regulatory professionals at global and European level, supporting both early-stage and marketed products. This role will further ensure compliance with the applicant's and/or marketing authorization holder's responsibilities under legislation or regulatory guidelines for assigned products in Italy. /p pThe Senior Director Regulatory Affairs is an essential member of the local Management Team, while also acting as a strong and active member of the International Regulatory Team. The candidate will provide regulatory support for assigned products and therapeutic areas and work cross-functionally with medical affairs, clinical development, marketing and other teams to support the development and execution of medical strategies and tactics. /p h3Further responsibilities include: /h3 ul liSupport global and regional RA as applicable with the preparation and follow-up for national scientific consultations and pre-submission meetings. /li licoordination of the creation of materials for risk mitigation activities and healthcare professional communication. /li liensuring that product packaging and related information are updated and maintained in accordance with regulatory requirements. /li lireview and approval of promotional materials.



/li liIn collaboration with regional and/or global RA organization represents the regulatory function at internal and external meetings, as applicable. /li liClose monitoring and analysis of all nationally relevant Italian regulatory guidelines and communication of updates and implications to both regional and global teams. /li liMaintain knowledge of complex Italian and EU regulatory requirements, contribute to the preparation of new regulatory guidelines wherever possible, comment on draft regulatory guidelines, and communicate changes to regulatory information to project teams and senior management locally and internationally. /li liparticipates in industry association groups and regulatory affairs professional societies. /li liinitiates or contributes to local and/or global process improvements that have a significant impact on the business. /li lileading the creation, maintenance, continuous improvement, training, evaluation, and follow-up of all regulatory-related procedures, including policies, SOPs, manuals, and work instructions, to meet local regulatory requirements. /li limanaging affiliate inspections and audits. /li limanaging quality defects, counterfeit or imitation products, and batch recalls. /li liserving as the information officer. /li liresponsible for distribution and wholesale licenses. /li limanaging local regulatory and regulatory compliance audits within the affiliate. /li limanagement and leadership responsibilities, as applicable. /li liProvide the vision and direction for the Regulatory Affairs organization at the country level, in line with Global / European Regulatory Affairs and the Italian affiliate's vision. /li liplans, monitors, allocates, and optimizes resources and budget with regard to portfolio development and regulatory changes. /li liensures a well-staffed and appropriately trained affiliate, as applicable. /li liadhere to Revolution Medicines Core Values and policies. /li liUnderstand the regulatory requirements for customer engagement by field-based employees.



/li /ul h3Required Education, Experience and Skills: /h3 ul liMaster’s / PhD degree in scientific or medical discipline. /li li10+ years of experience in regulatory leadership roles or in a similar role within the pharmaceutical or biotech industry. /li liStrong understanding of the regulatory framework in Italy and the EU. /li liKnowledge and experience within the oncology therapeutic area. /li liExcellent verbal and written communication skills in Italian and English. /li liProven ability to analyze and summarize scientific information effectively. /li liExcellent presentation skills, with the ability to effectively communicate complex scientific data to diverse audiences. /li liStrong networking skills with proven ability to successfully build and maintain relationships with Italian regulatory bodies and healthcare professionals. /li liIndependent and able to thrive in a fast-paced and dynamic environment. /li liWillingness to travel up to 30% of time. /li /ul h3Preferred Education, Experience and Skills: /h3 ul liPreferred experience in oncology. /li liExperience with both early and late-stage clinical assets as well as approved therapies. /li /ul pRevolution 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 CCPA Notice and Privacy Policy. For additional information, please contact /p pWe 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. /p pPlease 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 [email protected] /b email address. /p pIf you believe you’ve been contacted by someone impersonating a Revolution Medicines recruiter, please report it to so we can share these impersonations with our IT team for tracking and awareness. /p /p #J-18808-Ljbffr

📌 Senior Director, Regulatory Affairs, Italy (Italia)
🏢 Revolution Medicines
📍 Italia