Senior Manager - JP CA lead (IGTD)

1 Month ago • 10 Years + • $10,000,000 PA - $14,000,000 PA

Job Summary

Job Description

This role involves leading the Japan IGTD CA Team and overseeing clinical studies and evidence development projects for Philips Image-guided Therapy. Responsibilities include developing local clinical evidence strategies, interacting with regulatory bodies (MHLW/PMDA/KTLs), managing CRO services, reviewing clinical documentation, and overseeing clinical administration. The role requires staying informed of regulations and technologies relevant to endovascular therapeutics, ensuring GCP compliance, and aligning with local business needs. Additionally, the candidate will manage the team to proceed with plans and projects, providing interpretation of local regulations and reporting to the Head of Japan RA/CA and the head of IGTD CA/MA.
Must have:
  • 10+ years of experience in clinical operations.
  • Experience in medical device clinical studies.
  • Knowledge of PMD act, GCP, GPSP, ICH, and ISO13485.
  • Fluent in Japanese and English.
Good to have:
  • Working knowledge of EVT or cardiovascular medical devices.
Perks:
  • Incentives - 20%
  • Commuting allowance.
  • Social insurance (Employees' Pension Insurance, Health Insurance), and Labour Insurance (Employment Insurance, Industrial Accident Insurance).
  • Retirement benefit plan.
  • Various online training and support training after joining the company.
  • Internal recruitment system.

Job Details

Job Title

Senior Manager - JP CA lead (IGTD)

Job Description

Philips is a global leader in health technology, committed to improving billions of lives worldwide and striving to make the world healthier and more sustainable through innovation. Driven by the vision of a better tomorrow.

But it’s not just what we do, it’s who we are. We are 75,000, wonderfully unique individuals, with two things in common: An unwavering sense of purpose and a relentless determination to deliver on our customers’ needs. It’s what inspires us to create meaningful solutions – the kind that make a real difference – when it matters most.

The world and our customers’ needs are changing faster than ever before and while we are proud of what we do already, we know we can do more. That’s why we need you, to help us tackle increasingly complex challenges posed by ever evolving health and well-being needs.

Your role:

Exciting opportunity to lead the team working on Cardiac and Endovascular registration projects for Philips Image-guided Therapy, which includes novel technologies integrated by therapeutic devices and visualization systems.

  • Lead the Japan IGTD CA Team and all clinical studies and evidence development projects that the team is responsible for to proceed with the plan.
  • Lead developing local clinical evidence development strategy and strategic discussion with the local RA team and other related stakeholders, including Business Unit, R&D, and Market Access & Reimbursement to accelerate projects and fast serve patients.
  • Proactively identify risks within clinical evaluation strategies, plans, products and propose alternate approaches.
  • Provide interpretation of local regulations to BU partners and ensure necessary requirements are fully deployed.
  • Stay informed of new regulations and technologies relevant to endovascular therapeutics.
  • Plan and execute clinical evidence development, GCP compliance review of foreign operated clinical trials, and PMS study as a condition of approval according to the regulations and aligned with local business needs.
  • Manage interactions with MHLW/PMDA/KTLs and maintain a productive working relationship.
  • Manage CRO services to ensure meeting with Philips’ business needs and operational policies.
  • Review and approve clinical documentation according to the GCP/GPSP requirements.
  • Oversee clinical administration activities.
  • Report to the Head of Japan RA/CA as a solid line and the head of IGTD CA/MA as a dotted line.

You're the right fit if:

1. Experience.

  • +10 years’ experience in clinical operation including medical device.
  • Experience in the Study Manager role in medical device clinical studies and GCP compliance inspections by PMDA.
  • Maintains extensive knowledge of the PMD act, GCP ordinance, GPSP ordinance, ICH guidelines, and ISO13485.
  • Experience or working knowledge of EVT or any cardiovascular therapeutic medical devices.

2. Skills.

  • Self-motivated and able to prioritize handling multiple tasks/responsibilities.
  • Capable of thinking critically, logically, and strategically
  • Bachelor of Science Degree (Master preferred)
  • Fluent in Japanese and English

募集要項:

【契約期間】期間の定めなし 

【試用期間】試用期間あり(原則として入社日より6ヶ月)

【業務内容】(雇入れ直後)上記のとおり(変更の範囲)会社の定める業務

【就業場所】(雇入れ直後) 本社(麻布台ヒルズ)(変更の範囲)会社の定める就業場所

【就業時間】9:00-17:30 休憩時間:原則として12:00-13:00  

【勤務形態】ハイブリット(週3日オフィス出社、週2日までリモート勤務可能)               

【休日】毎週土曜日(所定休日)、日曜日(法定休日)、国民の祝日、年末年始(12月29日-1月4日) 

【休暇】初年度有給休暇 最大20日間(2年度~5年度 20日/6年度以降 25日 付与)、CareLeave(年間10日間)、Sick Leave(年間最大30日間)ほか 

【時間外労働】あり 

※ただし、管理職での採用の場合は、残業代は支給対象外(深夜勤務手当、休日深夜勤務手当の支給はあり) 

【給与】基本給 年収1000~1400万円 ご経験により考慮します 

【賞与】インセンティブ 20%

※インセンティブは毎年3月に支給。(会社業績、部門業績、個人評価によって変動あり) 

※年度途中入社者は対象期間中日割計算あり 

【手当】通勤手当の支給あり 

【加入保険】社会保険(厚生年金保険、健康保険)・労働保険(雇用保険、労災保険) 

【退職金制度】退職一時金および確定拠出年金の2本立て 

【研修制度】 各種オンライン研修、入社後のサポート研修あり

【社内公募制度あり】社内でのキャリアチェンジを推進する制度として社内公募制度の体制あり 

【その他】PhiliFlexポイント:72,000 ポイント(1ポイント=1円) 

About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
• Learn more about our business.
• Discover our rich and exciting history.
• Learn more about our purpose.

If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our commitment to diversity and inclusion here.

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About The Company

At Philips, we believe that every human matters. As a global health-tech leader, we focus on improving people’s health and wellbeing through meaningful innovation. The people who work here share our passion and are motivated to bring this purpose to life.For more than 130 years, we have been creating technologies and innovations that improve people's lives and support healthcare practitioners. Headquartered in the Netherlands and operating in more than 100 countries globally, we focus our advanced technology and deep clinical and consumer insights on Precision Diagnosis, Image Guided Therapy, Enterprise Informatics, Monitoring/ Connected Care, Sleep & Respiratory Care and Personal Health.Together, we deliver better care for more people because we believe that every human matters.

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