About this opportunity
Barrington James lists this Associate Director/Director Program Management opportunity in des plaines, Illinois. Review the employer’s description below for duties, qualifications and application requirements.
Job description
Associate Director/Director Program Management
Greater Chicago Area - Hybrid
We’re exclusively partnered with a biopharmaceutical company operating a unique model and are currently seeking an Associate Director / Director of Program Management . This is a fantastic opportunity to join an organization with a diverse portfolio spanning both biologics and small molecules, covering end-to-end development through to commercialization.
The Global Project Leader will support drug development programs across multiple therapeutic areas, providing project leadership and oversight within a cross-functional, highly matrixed organization. This individual will contribute to the development of comprehensive, integrated project plans based on robust scientific data to support regulatory submissions and secure approval aligned with the Target Product Profile.
Key Responsibilities
Support the management of drug development projects from kick-off through to approval, including assisting in the development of integrated project plans, establishing timelines, and ensuring alignment with strategic objectives.
Lead projects in a fast-paced environment, fostering collaboration and ensuring high-quality execution while maintaining strong team dynamics and sustainable performance.
Support the PMO function in designing and implementing effective tools, templates, and processes to drive continuous improvement, increase efficiency, and streamline operations across the organization.
Provide regular project status updates to stakeholders and senior leadership; establish reporting processes to ensure transparency around progress, risks, and key milestones in line with PMO governance.
Support the leadership of highly matrixed, cross-functional global Joint Project Teams (JPTs) through development to approval, including scenario planning (approval strategy, product narrative, value proposition, benefit-risk assessment, and mitigation strategies).
Lead the development and maintenance of compound development strategies, ensuring delivery within approved budgets and timelines in close collaboration with cross-functional teams.
Motivate and challenge team members to ensure all issues are addressed, incorporating functional input into strategy and execution plans to meet asset needs.
Identify potential risks and lead contingency planning; drive problem-solving within the JPT using structured decision-making tools and techniques to ensure effective and timely decisions.
Qualifications & Skills
Degree in Life Sciences and/or Project Management
Minimum of 7 years’ experience within industry, academia, or consulting
Strong understanding of the end-to-end drug development process, with prior experience in biopharmaceutical project management
Proven ability to work cross-functionally with interdisciplinary teams to optimize resources and deliver development programs
Commercially minded, with experience managing budgets and resources and a track record of progressing programs through development to registration and beyond
Strong leadership and communication skills, with a results-oriented mindset
Demonstrated problem-solving ability, with experience developing innovative solutions in complex environments
Excellent project planning and tracking skills, with strong strategic thinking and contingency planning capabilities
Proficiency in MS Project, Smartsheet, Gantt planning, PowerPoint, SharePoint, Excel, and other project management tools
Solid development acumen, with experience leading large, cross-functional teams across complex drug development programs (e.g., injectables, drug-device combinations, multiple formulations and delivery methods), with the ability to maintain a “big picture” perspective
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Worksite address
des plaines, IL, 60019, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.