Japon / PMDA

Marketing ManagerJapan Operations

Now Hiring • Tokyo, Japan

Japon / PMDA
Marketing ManagerJapan Operations
WHAT THIS PAGE COVERS
1
The Role in Japan
2
Required Qualifications
3
Strong Assets
European CRO for medical devices, aligned with Regulation (EU) 2017/745.
Trusted by manufacturers

Leading medical device teams work with Eclevar

Terumo
Nihon Kohden
Vygon
Coloplast
Asahi Intecc

Take ownership of Eclevar's digital presence in Japan. Build our brand awareness, manage targeted B2B campaigns, and orchestrate high-impact webinars for the medical device industry.

Tokyo, Japan (Hybrid) Full-time B2B Marketing MedTech / CRO

The Role in Japan

You will be the driving force behind Eclevar's marketing strategy in Japan. Working closely with our global team in Paris, you will localize our messaging, manage our digital channels, and create compelling campaigns to generate qualified leads among Japanese medical device manufacturers.

  • Manage and grow the Eclevar Japan LinkedIn presence with targeted content.
  • Execute B2B digital marketing campaigns to drive engagement and lead generation.
  • Monitor digital KPIs and optimize campaign performance.
  • Plan, promote, and execute Japanese-language webinars with our experts.
  • Coordinate Eclevar's presence at major local MedTech conferences and trade shows.
  • Manage post-event follow-ups to nurture acquired leads.
  • Translate and adapt global marketing materials (white papers, case studies) for the Japanese market.
  • Maintain and update the Japanese section of the corporate website.
  • Ensure all messaging aligns with local business culture and regulatory nuances.
  • Develop localized pitch decks and sales collateral for the business development team.
  • Conduct market research to identify new opportunities in the Japanese MedTech landscape.
  • Collaborate with global marketing to ensure brand consistency.

Required Qualifications

  • Minimum 3-5 years of experience in B2B marketing or digital marketing.
  • Native-level Japanese and professional fluency in English (mandatory for global alignment).
  • Proven track record in managing corporate LinkedIn accounts and webinar platforms (Zoom, Teams).
  • Experience with CMS (WordPress) and CRM/Marketing Automation tools (HubSpot, Salesforce).
  • Strong copywriting and content adaptation skills.

Strong Assets

  • Prior marketing experience within the Healthcare, Life Sciences, or Medical Device industry.
  • Familiarity with graphic design and video editing tools (Adobe Creative Cloud, Canva).
  • Experience working in a fast-paced, international scale-up environment.
  • Existing understanding of clinical research or regulatory affairs terminology.
Expertise and recognition

A European team of former notified body reviewers

The people who build your evidence have sat on the other side of the table.

EUCROF Platinum Award 2026
EUCROF Platinum Award 2026xShare Open Call for Clinical Research, co-funded by the European Union
Dr Mark Da CostaDr Mark Da CostaChief Medical OfficerTÜV SÜD
Dr Nikhil KhadabadiDr Nikhil KhadabadiHead of Clinical EvidenceEU MDR
Pierre-Marie BoutanquoiPierre-Marie BoutanquoiDirector of Clinical OperationsISO 14155
FAQ

Questions sponsors ask first

Why join Eclevar?

Take the lead on all local marketing initiatives with the freedom to test new ideas and strategies.

Ready to drive our growth in Japan?

Send your CV/Resume and a brief introduction highlighting your B2B digital marketing experience.

Official content

Our content, signed Eclevar.

Whitepapers and publications produced by our teams with our notified body partners.

Whitepaper by BSI and Eclevar on the EU MDR
Whitepaper · BSI × Eclevar

A BSI and Eclevar whitepaper on the EU MDR.

Written with Notified Body BSI: a practical reading of the clinical evidence expectations under EU MDR 2017/745, the same evidence your file has to support.

Start the conversation

Tell us where your evidence stands today

Send us the device, the claim and the deadline. You get a written answer within 24 hours.

Your documents are reviewed confidentially. An NDA can be signed before we receive any technical or clinical information.

Reforming Clinical Evaluation of Medical Devices in Europe