Sanofi

Sanofi

Posted via Workday

T1D Medical Manager

Apply by Dec 4, 2026

Posted Sep 4, 2026

Role at a glance

Salary
Not Disclosed
Location
Tokyo, Japan
Work arrangement
Hybrid
Employment
Full-time
Experience
Prior experience of clinical trials/studies management and understanding of relevant guidelines (e.g. GCP, Ethics guideline) required Desirable – ■ Min 5-year experience in R&D and / or Medical in pharmaceutical companies ■ Have experience at least two years of MSL or three years of Medical Manager/Medical Advisor’s role
Education
Advanced degree (MD, PhD, PharmD, DNP in medical specialty) preferred, or other relevant life science degree (RS/MS) with healthcare...

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Role Summary

AI-generated

The T1D Medical Manager supports and executes medical activities for autoimmune Type 1 Diabetes in Japan, aligned with the overall medical strategy. The role contributes to scientific planning, medical communication, stakeholder engagement, and studies related to teplizumab and other immunotherapeutics.

What You'll Do

  • Support development and execution of the Japan Medical Plan, provide scientific input on promotional materials, and collaborate on...
  • Assist with publication planning and execution, develop medical content, engage with KOLs and scientific societies, present data at...
  • Plan and execute company-sponsored studies and externally sponsored collaborations, including post-approval studies.
  • Review and support Investigator-Sponsored Studies and analyze real-world data with internal and external experts.

Generated from the employer's posting. Verify important details before applying.

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Qualifications

Required: Other relevant life science degree (RS/MS) with a healthcare specialty; experience managing clinical trials/studies and understanding relevant guidelines such as GCP and Ethics guidelines. Must be fluent in Japanese and have business-level English reading and writing skills. Skills include therapeutic-area and medical research and development knowledge, statistical and data interpretation, scientific paper writing, strategic understanding, written communication and presentation, and maintaining effective relationships with healthcare professionals.

Required

  • Other relevant life science degree (RS/MS) with healthcare specialty
  • Prior experience of clinical trials/studies management and understanding of relevant guidelines (e.g. GCP, Ethics guideline)
  • Fluent in Japanese and business-level English (reading/writing)
  • Scientific and technical knowledge in the therapeutic area
  • Statistical and data interpretation, analytical thinking, and understanding of causation
  • Experience in writing scientific medical papers (as appropriate)
  • Written communication and presentation skills
  • Ability to establish and maintain effective relationships serving HCP needs

Preferred

  • Advanced degree (MD, PhD, PharmD, DNP in medical specialty)
  • Min 5-year experience in R&D and / or Medical in pharmaceutical companies
  • At least two years of MSL experience or three years of Medical Manager/Medical Advisor’s role
  • Understanding of health economics

Original job description

Content provided by the employer

Job title: T1D Medical Manager

  • Location: Tokyo


Reporting to the T1D (Type 1 Diabetes) Medical Head, and providing guidance to Medical Advisors, the T1D Medical Manager is responsible for supporting and executing medical activities focused on autoimmune Type 1 Diabetes. This role ensures the timely and effective execution of initiatives that align with the overall medical strategy for T1D. The Medical Manager contributes to scientific planning, medical content development, and external stakeholder engagement, supporting the launch and ongoing success of teplizumab and other immunotherapeutics.

Key accountabilities

Support Medical Strategy Execution (20%)

■ Support the T1D Medical Head in developing and executing the Japan Medical Plan.

■ Provide scientific input for promotional materials in collaboration with marketing.

■ Collaborate with cross-functional teams to address unsolicited medical requests.

■ Assist in regulatory interactions and development planning.

■ Identify unmet medical needs to support lifecycle opportunities.

Support Medical Communication/Publication and Exchange (30%)

■ Assist in publication planning and execution (articles, congresses, symposia).

■ Engage with KOLs and scientific societies to build networks.

■ Support field strategy development with MSLs and global medical teams.

■ Develop medical contents

■ Present data at advisory boards and scientific meetings.

■ Collect and share medical insights with the Medical Head.

Support Medical-related Studies (50%)

■ Generate evidence by planning and executing company-sponsored studies and externally sponsored collaborations.

■ Collaborate on post-approval study planning and execution.

■ Review and support Investigator-Sponsored Studies (ISSs).

■ Analyze real-world data with internal and external experts.

Context of the job/major challenges

■ Operate independently while providing guidance to Medical Advisors.

■ Navigate complex regulatory environments and ensure compliance.

■ Manage national/international travel and remote work (40% remote, 60% onsite).

■ Maintain scientific integrity in non-promotional activities.

Requirements

Education/experience

■ Advanced degree (MD, PhD, PharmD, DNP in medical specialty) preferred, or other relevant life science degree (RS/MS) with healthcare specialty required

■ Prior experience of clinical trials/studies management and understanding of relevant guidelines (e.g. GCP, Ethics guideline) required

Desirable –

■ Min 5-year experience in R&D and / or Medical in pharmaceutical companies

■ Have experience at least two years of MSL or three years of Medical Manager/Medical Advisor’s role

■ Understanding of health economics

■ Scientific and Technical knowledge in Therapeutic area

SKILLS/KNOWLEDGE

■ Scientific acumen: Therapeutic area knowledge, experience in medical research & development

■ Statistical & data interpretation: Analytical thinking and understanding of causation

■ Medical paper writing: Experience in writing of scientific medical papers (as appropriate)

■ Strategic acumen: Understanding strategic needs of affiliate organization important for completion of tasks

■ Must be fluent in Japanese and business level English (reading/writing)

■ Process Related Core Competencies

■ Focus on scientific exchange: Dedicated to serving HCP needs, feedback, establishes and maintains effective relationships

■ Effective Communication: Written communications and presentation skills

■ Other skills: Approachability, Interpersonal savvy

Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

Sanofi

About the company

Sanofi

Large Enterprise

Sanofi is a global healthcare leader committed to promoting health and well-being through the development of innovative medicines, vaccines, and therapeutic solutions. With a diverse portfolio that spans multiple therapeutic areas, including diabetes, oncology, and immunology, Sanofi is dedicated to addressing pressing health challenges and improving patient outcomes worldwide. Headquartered in France, the company employs over 100,000 individuals across more than 100 countries, fostering a culture of collaboration and scientific excellence to drive advancements in healthcare.