Recruitment background

Senior Program Manager · Cancer Screening

루닛|2026. 10. 20. 게시|
2

공고 요약

경력10년~19년
채용 유형정규직
학력무관
지역서울
마감일상시채용
출처원티드

주요 업무

  • 회사 전략과 제품 목표를 프로그램 목표, 주요 마일스톤 및 통합 실행계획으로 구체화

  • 제품 개발, 검증, 규제 대응 준비, 출시 및 종료까지 전 과정의 프로그램 리드

  • 제품관리, AI 연구, 엔지니어링, 데이터, 임상, 규제, 품질보증, 사업 조직 등 여러 기능 조직과 협업

  • 복수 프로젝트와 워크스트림을 하나의 프로그램으로 통합하고 의존성, 리스크, 이슈 및 주요 일정 관리

  • 범위, 일정, 자원, 품질 및 규제 요구사항을 고려한 프로그램 실행 조율

  • 프로젝트와 기능 조직 간 우선순위 및 트레이드오프 조율, 적시 의사결정 지원

  • 복잡한 이슈 구조화 및 이해관계자 합의 형성

  • 프로그램 거버넌스 수립 및 운영, 경영진과 주요 이해관계자에게 진행 현황, 리스크, 의존성 및 주요 의사결정 공유

  • 프로그램 관리 프로세스와 거버넌스 개선, 조직 실행 역량 강화

자격요건

  • 복잡한 여러 기능 조직 간 프로그램 리드를 포함한 관련 경력 10년 이상

  • 규제 대상 제품의 개발 및 상용화 전 과정 프로그램 관리 경험

  • 프로그램 목표 달성을 위한 상호 의존적인 프로젝트와 워크스트림 통합 경험

  • 제품 생애주기에 대한 이해 및 프로그램 수준의 범위, 일정, 리스크, 의존성, 이해관계자 관리 역량

  • 규제, 품질, 기술 및 사업 요구사항을 함께 고려하는 환경에서의 프로그램 리드 경험

  • 다양한 기능 조직 및 고위 이해관계자와의 원활한 소통·협업 역량과 의사결정 지원 능력

  • 영어 전문 수준의 의사소통 능력

우대사항

  • 외국어 능통자

복리후생

  • 건강검진 지원

  • 자기계발 지원

  • 스톡옵션

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공고 원문

소개

"Conquering cancer through AI" Lunit, a portmanteau of ‘Learning unit,’ is a medical AI software company devoted to providing AI-powered total cancer care. Our AI solutions help discover cancer and predict cancer treatment outcomes, achieving timely and individually-tailored cancer treatment. [About the position] • The Senior Program Manager within Lunit’s PMO translates company strategy and product objectives into clear program objectives and execution plans. Working closely with cross-functional teams, this role leads end-to-end programs across the entire product lifecycle, from product development and validation through regulatory readiness, launch, and phase-out. • The Senior Program Manager identifies and manages program-level dependencies and risks, aligns priorities and trade-offs, and enables effective decision-making and collaboration to achieve the program’s strategic objectives and intended outcomes.

주요업무

• Translate company strategy and product objectives into clear program objectives, key milestones, and integrated execution plans • Lead end-to-end programs across product development, validation, regulatory readiness, launch, and phase-out in collaboration with Product Management, AI Research, Engineering, Data, Clinical, Regulatory Affairs, Quality Assurance, Commercial, and other cross-functional teams • Integrate and manage multiple projects and workstreams as a cohesive program, including cross-functional dependencies, risks, issues, and key timelines • Coordinate program execution by considering scope, timelines, resources, quality, and regulatory requirements holistically • Align priorities and trade-offs across projects and functions and facilitate timely decision-making • Structure complex issues and build stakeholder alignment to support effective program execution • Establish and operate program governance, providing senior leadership and key stakeholders with clear visibility into program status, risks, dependencies, and key decisions • Continuously improve program management processes and governance and contribute to strengthening organizational execution capabilities

자격요건

• 10+ years of relevant professional experience, including experience leading complex, cross-functional programs • Demonstrated experience leading end-to-end program management across the development and commercialization of regulated products • Proven experience integrating multiple interdependent projects and workstreams to achieve program-level objectives and intended outcomes • Strong understanding of the product lifecycle and the ability to manage scope, schedule, risk, dependencies, and stakeholders at the program level • Experience leading programs in environments where regulatory, quality, technical, and business requirements must be considered together • Strong communication and collaboration skills with diverse functional teams and senior stakeholders, with the ability to support effective decision-making • Professional proficiency in English

우대사항

• Experience leading programs across medical device product development, regulatory approval, and commercialization • Experience with Software as a Medical Device (SaMD), AI/ML-enabled medical devices, or Digital Health products • Understanding of the medical device Product Development Lifecycle, Design Controls, Verification & Validation, Quality Management Systems, and Regulatory Processes • Experience with global cross-functional programs or PMO/portfolio management

혜택 및 복지

• The office is at a very convenient location, just a minute away from Gangnam Station Exit 3. • Meal Allowance is provided (up to 12,000 KRW per meal) when working at the office. • Latest computer models, such as Macs and 4K monitors are provided and can be renewed every three years. • Seminar registration fees and book purchases are covered. • Regular in-house AI and medical seminars are held. • In-house English lessons (aka Luniversal) are provided for English development. • Access to high-quality AI learning resources & deep learning DevOps system. • Up to 1.2 million KRW worth of benefits points can be claimed annually. • Holiday Allowances are provided in the form of gifts or vouchers for Korean National holidays, Seollal and Chuseok. • Congratulatory and Condolence allowances, along with paid time off are provided. • Annual medical checkups and employee accident insurance are provided.

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