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Bristol Myers Squibb

Makes drugs for cancer, blood and immune diseases

Associate Director - Program Management

Program ManagementConfirmed live in the last 24 hours
Full-timeWarsaw, PolandIn-person

About the Job

Requirements

  • An advanced degree in Life Sciences, Chemical Sciences, Physical Sciences, or another relevant discipline is required. BS/MS degrees in a scientific discipline combined with 8+ years of drug development experience will also be considered.
  • The ideal candidate will have 10+ years of experience in the biotech, pharmaceutical, or health care industry.
  • Experience in project or portfolio management, or leadership of cross-functional matrix teams, is a plus.
  • Demonstrated track record of planning and managing complex programs in early- or late-phase drug development, solid understanding of a disease area and the drug development pathway, and ability to facilitate and contribute to strategic discussions.
  • Expert understanding of end-to-end drug development processes and product value assessment.
  • Leadership skills including situational leadership and the ability to lead a team of experts and influence without authority.
  • Demonstrated ability to lead matrix teams, work strategically with the Global Program Lead, and delve into details to resolve issues and challenges.
  • Experience with commonly used project management tools, including Microsoft Project.
  • Ability to communicate clearly, integrate and succinctly summarize project components, and tailor messages effectively to audiences including senior leaders.
  • Ability to resolve complex problems and manage difficult stakeholder situations.
  • Ability to lead critical path analyses and scenario planning.
  • Excellent project management skills to drive execution while balancing speed, quality, and cost.
  • Full professional proficiency in English, with excellent written and verbal skills.
  • Strong organization, attention to detail, problem-solving capability, and business acumen; ability to manage competing priorities and objectively guide the team toward value-maximizing decisions while maintaining an end-to-end cross-functional view.

Responsibilities

  • Partner with the Global Program Lead and Global Project Manager to co-lead strategic and operational planning and decision-making for a Global Program Team in early- and/or late-stage development.
  • Partner with the Global Program Lead and Global Project Manager to lead Global Program Team sub-teams and drive development of integrated, efficient, cross-functional program execution plans.
  • Coordinate and plan Global Program Team activities, including milestone setting, budget forecasting, resource planning, scenario planning, and development of an integrated program plan based on cross-functional inputs and assumptions.
  • Facilitate team goal setting and tracking to ensure adherence to the plan and strategy, and prepare for the year-end team evaluation process.
  • Manage Global Program Team sub-teams, track integrated deliverables, and prepare the team for governance interactions at program inflection points.
  • Lead integrated cross-functional planning across functional plans and strategies; define program operational strategy; and manage timelines, budget, quality, and risk assessment and mitigation.
  • Provide project management and operational expertise to drive the Global Program Team and sub-teams toward execution excellence, shape project strategy, and support optimal decisions for the broader portfolio.
  • Be accountable for one or more Global Program Teams and associated moderate-complexity sub-teams in early- or late-stage development; operate autonomously day to day, or support workstreams of a large, highly complex late-stage team under a Senior Project Manager.
  • Create and maintain cross-functional development plans, timelines, and budgets for each program, and ensure progress against plan.
  • Facilitate science-based business decisions, including generating development scenarios or options as needed and highlighting interdependencies and downstream impacts, including timelines and budget, of strategic decisions.
  • Identify risks proactively and ensure mitigation plans are implemented.
  • Communicate transparently and promptly with the team and stakeholders.
  • Work with the Global Program Lead to foster a high-performing team, monitor team health and operating efficiency, and lead the creation of team norms and operating principles focused on cross-functional input and accountability.
  • Coordinate resource and budget planning across functions to ensure adequate project resources and appropriately highlight changes.
  • Advise on governance expectations and prepare for key decision-point discussions, emphasizing cross-functional input and rigorous debate.
  • Work closely with strategic alliance partners on jointly developed projects.
  • Coach project team members and project management colleagues to drive excellence and accountability, and develop the talent pipeline for Global Program Team membership.
  • Act as a change agent for continuous improvement and transformational initiatives within the project management function.
  • Guide the Global Program Team and manage preparation of high-quality documents and presentations for governance committee reviews.
  • Ensure appropriate Global Program Team membership as the program progresses.

Desired Qualifications

  • A Ph.D. in Life Sciences, Chemical Sciences, Physical Sciences, or another relevant discipline is desirable.
  • Project Management Professional (PMP) certification is desirable.

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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