Associate Director, Drug Development Project Management Lead

16 hours ago

Cambridge, Massachusetts, United States Bristol-Myers Squibb Full time
Job Summary

We are seeking an experienced Associate Director, Drug Development Project Management to join our team at Bristol-Myers Squibb. As a key member of our Global Program Team, you will be responsible for leading the strategic and operational planning and decision-making process for early and late development programs.

Key Responsibilities
  • Partner with the Global Program Lead and Global Project Manager to co-lead the strategic and operational planning and decision-making process for early and late development programs.
  • Provide content expertise to the timing, costs, and resources required for development programs and successfully deliver program milestones and goals.
  • Ensure cross-functional teams operate effectively, fostering positive team dynamics and championing BMS' operating model.
  • Coordinate and plan activities for the Global Program Team, including milestone setting, budget forecasting, resource planning, scenario planning, and developing an integrated program plan based on cross-functional inputs and assumptions.
  • Facilitate team goal setting and tracking to ensure adherence to plan and strategy and in preparation for end of year team evaluation process.
  • Manage all associated Global Program Team sub-teams and tracking integrated deliverables and preparing the GPT for governance interactions at program inflection points.
  • Accountable for integrated cross-functional planning bringing together diverse functional plans and strategies, definition of the program operational strategy, management of timelines, budget, quality, and risk assessment and mitigation.
  • Work independently to provide best in class operations and project management expertise to drive the GPT and sub-teams toward execution excellence.
  • Provide an independent voice to shape the overall project strategy and drive optimal decisions for the broader portfolio value.
Requirements
  • Advanced degree (Ph.D. desirable) in Life Sciences, Chemical Sciences, Physical Sciences, or other relevant discipline.
  • PMP certification is desirable.
  • BS/MS degrees in a scientific discipline in combination with 8+ years of drug development experience will be considered.
  • The ideal candidate will have 10+ years of experience in biotech/pharmaceutical/health care industry; experience in project/portfolio management or leadership of cross-functional matrix teams is a plus.
  • Proven track record of planning and managing complex programs in early and/or late phase drug development with solid understanding of disease area and drug development pathway with the ability to facilitate and contribute to strategic discussions.
  • Expert understanding of the end-to-end processes in drug development and product value assessment.
  • Leadership skills including situational leadership, ability to lead a team of experts and influence without authority.
  • Demonstrated ability to lead matrix teams, knows how to work at the strategic level with the GPL and when to delve deeper to resolve issues and challenges.
  • Experience with commonly used project management tools including but not limited to Microsoft project.
  • Strong communicator able to integrate and succinctly summarize the various parts of a project and effectively tailor messages to audience including senior leaders.
  • Guides GPT and manages preparation of high-quality documents and presentations for review at governance committees.
  • Ensures appropriate GPT membership during the progression of the program.
  • Ability to resolve complex problems and manage difficult stakeholder situations.
  • Ability to lead the development of critical path analyses and scenario planning.
  • Excellent Project Management Skills - drives execution while balancing speed, quality, and cost.
  • Excellent written and verbal skills, (including full professional English proficiency).
What We Offer

Bristol-Myers Squibb offers a competitive compensation package, including a starting salary range of $169,000 - $211,000, plus incentive cash and stock opportunities (based on eligibility). We also offer a comprehensive benefits package, including medical, pharmacy, dental and vision care, wellbeing support, financial well-being resources, and work-life programs.

We are an equal opportunity employer and welcome applications from diverse candidates. If you are passionate about drug development and project management, and have the skills and experience to succeed in this role, we encourage you to apply.

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