About this Medical Operations Manager, Japan role at Revolution Medicines
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.
The Opportunity:
We are seeking a highly motivated and experienced professional to join our team as a Medical Operations (MO) Manager. Reporting to the Head of Japan Medical Affairs, this role will be responsible for managing medical events, contracting, vendor oversight, and budget control in close partnership with Global Medical Affairs (GMA) and regional stakeholders. MO Manger will also support to establish governance frameworks and cross-functional medical governance initiatives with Head of Japan Medical Affairs.
Key Responsibilities:
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Oversee the execution of MA projects and initiatives, ensuring timely delivery and alignment with business priorities.
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Lead contract management activities, including negotiation, execution, and tracking for MA vendors, consultants, and external partners.
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Contribute to logistical planning and execution of medical congress activities in partnership with internal stakeholders, ensuring seamless coordination of medical presence, booth activities, and KOL engagements.
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Support the planning and execution of advisory boards, symposia, and other key medical events, including contracting, compliance oversight, and logistics management.
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Work closely with Legal, Compliance, Regulatory, and Finance teams to ensure MA operations align with company policies and external regulations.
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Ensure medical activities align with corporate policies and external regulatory guidance, including MHLW, PMDA, JPMA, ICH, GVP, and other relevant regulations.
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Support to establish comprehensive Medical Governance framework to support strategic and operational excellence across Regional and GMA.
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Improvement efforts to streamline governance frameworks and enhance efficiency with MA Operations.
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Monitor regional MRC, ensuring efficient and compliant medical review of materials, communications, and scientific content.
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Support digital transformation initiatives within MA, including the implementation and optimization of medical systems, databases, and reporting tools.
Required Skills, Experience and Education:
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Minimum 5 years of experience in MA or related functions in the pharmaceutical or biotech industry.
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Strong background in Medical Governance, Compliance, Regulatory Affairs, or Medical Operations.
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Deep knowledge of global and local regulatory requirements for MA, including MHLW, PMDA, JPMA, ICH, GVP, and industry best practices.
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Experience developing governance frameworks to support medical organizations.
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Experience leading MRC or similar governance structures.
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Fluency in Japanese and business level English
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Ability to navigate complex regulatory and legal environments and advise teams on best governance practices.
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Strong interpersonal, communication, and leadership skills with the ability to influence cross-functional stakeholders.
Preferred Skills:
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Advanced scientific or medical degrees (MD, RPh, PhD) preferred; MS or equivalent experience in biomedical sciences or business management field will also be considered.
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Experience working in global biotech/pharmaceutical environments, supporting multiple departments or teams.
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Expertise in digital platforms for compliance tracking, document management, and governance reporting.
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