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Johnson & Johnson

Makes prescription drugs and medical devices

Director Project Team Leader

Program ManagementConfirmed live in the last 24 hours
Full-timeNo 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 China and/or Japan local practices, policy, and regulation, and insight into requirements for market success, including commercial objectives.
  • A strong track record of delivering as part of a cross-functional project team.
  • Strong analytical and problem-solving skills, including the ability to synthesize complex information and make 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 Chinese and/or Japanese.
  • A scientific background and an advanced degree in a relevant discipline, such as medical, pharmacy, regulatory, quantitative sciences, or business.

Responsibilities

  • Lead country-level cross-functional Project Teams as an extension of the CDT, ensuring Japan and China contribute to global strategy rather than only executing downstream.
  • Ensure a unified local voice, including alignment between local research and development and commercial teams, to provide input to global CDTs on China and Japan project strategies.
  • Generate, synthesize, and proactively position high-quality Japan and China insights across regulatory, clinical, operational, portfolio, and commercial interfaces.
  • Partner with the CDT, research and development teams in China and Japan, and commercial teams to translate global strategy into robust, scenario-based country delivery strategies that enable commercial success, 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 resolution of critical project issues arising in research and development in China or Japan, aligned with local or regional commercial teams and global CDTs.
  • Maintain ownership of country-level research and development governance inputs, ensuring decision traceability and strategic coherence.
  • Represent the country in the CDT as an research and development contributor and extended CDT member.
  • Act as a strategic interface and be accountable for execution among the CDTL, PDL, PML, RPM, and CPM; country research and development functions; and country non-research-and-development stakeholders, including MAF, NPP, MA, and BU.
  • Foster a unified team mindset across country Project Teams, aligned with 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 mindsets, 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 China and Japan, decision logs linked to global governance milestones, and communication records aligned with CDT and commercial decisions.
  • Represent research and development externally as appropriate, including 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 a TA lead only, provide TA-level expertise, act as the primary point of contact for TA stakeholders, and coach junior Project Team Leaders.

Desired Qualifications

  • Direct or matrixed people-management experience is preferred.
  • MD, PhD, PharmD, or MBA is strongly preferred.
  • Agile decision making.
  • Agility jumps.
  • Analytics insights.
  • Budget management.
  • Business behavior.
  • Business savvy.
  • Continuous improvement.
  • Leadership.
  • Organizational project management.
  • Program management.
  • Project management methodology.
  • Project management office.
  • Project management tools.
  • Project reporting.
  • Statement of work.
  • Tactical planning.
  • Technical credibility.

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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