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Johnson & Johnson

Makes prescription drugs and medical devices

Innovative Medicine R&D - Multiple Teams

Clinical Research OperationsConfirmed live in the last 24 hours
Full-timeChiyoda City, Tokyo, JapanNo salary listedHybrid

About the Job

Requirements

  • At least 8 years of experience in drug development, including 3 years leading cross-functional matrix teams within a global research and development organization.
  • Thorough knowledge of global drug development and registration, with deep understanding of pharmaceutical portfolio risk management.
  • In-depth knowledge of Japan local practice, policy, and regulation, and insight into requirements for market success and commercial objectives.
  • A strong track record delivering as part of a cross-functional project team.
  • Strong analytical and problem-solving skills, including synthesizing complex information and making sound judgments.
  • Ability to make informed decisions under uncertainty and take ownership to drive results.
  • Strategic thinking, business acumen, and an enterprise mindset.
  • Ability to collaborate, influence, and lead across teams in a matrix environment.
  • Stakeholder management, communication, negotiation, and project management skills.
  • Cultural agility and ability to navigate complex organizational environments.
  • Ability to combine strategic vision with execution to drive change and deliver impact.
  • Fluency in written and spoken English and Japanese.
  • A scientific background with an advanced degree in a relevant discipline, such as medical, pharmaceutical, regulatory, quantitative sciences, or business.

Responsibilities

  • Lead country-level cross-functional project teams as an extension of the CDT, ensuring Japan functions contribute to global strategy.
  • Align local research and development and commercial teams to provide input to global CDTs on project strategies for Japan.
  • Generate, synthesize, and proactively position Japan insights across regulatory, clinical, operational, portfolio, and commercial interfaces.
  • Partner with the CDT, research and development in Japan, and commercial teams to translate global strategy into robust, scenario-based country delivery strategies, enabling commercial success in Japan and addressing risk, feasibility, and value trade-offs.
  • Ensure disciplined execution of country plans and timely escalation of strategic, resourcing, and risk issues to the CDT and governance forums.
  • Lead critical project issue resolution arising in research and development in Japan in alignment with local or regional commercial teams and global CDTs.
  • Own country-level research and development governance inputs, ensuring decision traceability and strategic coherence.
  • Represent Japan research and development within the CDT as a topic-driven contributor and extended CDT member.
  • Serve as a strategic interface and be accountable for execution among the CDTL, PDL, PML, RPM, CPM, country research and development functions, and country non-research-and-development stakeholders (MAF, NPP, MA, BU).
  • Foster a one-team mindset across country project teams aligned to global and local priorities, accountability, and performance standards.
  • Provide senior cross-functional leadership in complex decision-making, conflict resolution, and strategic trade-offs.
  • Build teams with appropriate mindset, practices, and learning orientation, balancing rigor with agility and avoiding over-reliance on process for coordination.
  • Continuously improve team effectiveness, insight generation, and strategic contribution to the CDT.
  • Ensure fit-for-purpose, decision-oriented documentation, including strategic insight briefs, locally aligned input into the GFLS and ADP for Japan, decision logs linked to global governance milestones, and communication records aligned with CDT and commercial decisions.
  • Represent research and development externally as appropriate at scientific forums, health authority interactions, and key stakeholder engagements, consistent with asset strategy and governance expectations.
  • Ensure consistent and aligned research and development messaging across country, regional, and global stakeholders.
  • For TA lead only, provide therapeutic-area-level expertise, act as the primary point of contact for therapeutic area stakeholders, and coach junior Project Team Leaders.

Desired Qualifications

  • Direct or matrixed people management experience.
  • An MD, PhD, PharmD, or MBA.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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