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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Director, Program Management - Neuroscience

Program ManagementConfirmed live in the last 24 hours
Full-timeIn-person

About the Job

Requirements

  • An advanced degree in Life Sciences, Chemical Sciences, Physical Sciences, or another relevant discipline is required; an MS, MBA, or Ph.D. is desirable.
  • At least 12 years of industry experience, including at least 10 years of direct drug development program or project management experience.
  • Demonstrated experience in nearly all phases of research and drug development, including global regulatory submissions from IND/CTA through NDA/BLA/MAA/JNDA/NDA China and lifecycle management.
  • Proven success delivering complex program teams with high enterprise visibility and long-standing experience demonstrating strong matrix leadership abilities.
  • Strong executive presence and ability to present, influence, and gain alignment at senior governance and executive leadership levels.
  • Ability to manage interdependencies within therapeutic areas, disease areas, functions, and geographies.
  • Expertise in core program management methodologies and tools, especially planning and control, risk management, stakeholder management, and soft skills.
  • Ability to resolve critical technical and business problems and shape long-term development strategy for programs of enterprise significance.
  • Experience in various therapy areas is ideal.
  • PMP certification is desirable.

Responsibilities

  • Serve as a program management subject matter expert and key strategic partner to the Global Program Lead and Global Program Team, helping establish a high-performing team environment.
  • Execute the Integrated Development Plan for each asset indication in partnership with sub-teams and their leadership, ensuring alignment to the Target Product Profile and Integrated Development Plan and clarity on accountabilities.
  • Lead matrixed program management team members in creating and maintaining integrated cross-functional timelines for each asset indication in approved systems, including scenario plans to manage risk, assess alternative development strategies, and identify acceleration opportunities or cost savings.
  • Lead risk management at the Global Program Team and ensure sub-team risk management activities are performed, with timely escalation of high-probability, high-impact risks; deliver the risk management plan and mitigation strategies.
  • Monitor high-level direct budget and resource health for assigned assets and indications, maintain visibility, and advocate for resources needed to deliver the Integrated Development Plan as approved through governance.
  • Provide program management subject matter expertise in leadership discussions and governance stage gates.
  • Support Global Program Team annual objectives and budget planning, including annual and long-term portfolio processes.
  • Support Development and Delivery Program Management Portfolio Leads with asset or portfolio content as required.
  • Foster cross-functional thinking to shape program strategy and drive optimal decisions for the broader portfolio.
  • Lead as a change agent and represent the Development and Delivery Program Management department's vision and ways of working.
  • May serve as a matrix manager for Program Management resources assigned to the asset.
  • May have direct line management responsibility for Program Management team members aligned to asset indications.
  • May serve as a trusted deputy to the Global Program Lead.

Desired Qualifications

  • PMP certification.
  • Experience in various therapy areas.

About the Company

Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Bristol Myers Squibb discovers, develops and sells prescription medicines for serious illnesses, including cancer, blood disorders, immune diseases and heart disease, for patients treated by doctors and hospitals around the world. Its best-known drug is Opdivo, an immunotherapy that helps the body's own immune system find and attack many kinds of cancer. Researchers develop drug candidates in its labs or bring them in through acquisitions and partnerships, then test them in clinical trials to win regulatory approval. The company makes and markets the approved medicines and earns its revenue from sales of patent-protected drugs. Its roots go back to a business founded in 1887, and it is based in Lawrence Township, New Jersey.

Company size
10,001+
Company stage
IPO
Headquarters
Lawrence Township, NJ
Founded
1887

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