Jobs for People with MS: National MS Society

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.

• • 3 years' experience in people management.

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

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.

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