Associate Director/Director Program Management in Des Plaines

Energy Jobline ZR; Des Plaines (IL); Hybrid; USD 180,000 - 230,000; Full time

Job summary

Energy Jobline ZR in the Greater Chicago Area (hybrid) is seeking an Associate Director/Director of Program Management to lead drug development programs across multiple therapeutic areas, coordinating cross‑functional teams from development through to regulatory submission and commercialization.

The role requires strong leadership, strategic planning, and the ability to drive complex projects in a matrixed organization.

Qualifications

• 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 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 strategic thinking and contingency planning capabilities.

Responsibilities

• Support management of drug development projects from kick‑off through to approval, developing integrated project plans and timelines.
• Lead projects in a fast‑paced environment with high‑quality execution and strong team dynamics.
• Support PMO in designing and implementing tools, templates, and processes to drive efficiency and streamline operations.
• Provide regular project status updates to stakeholders and senior leadership; establish reporting processes for transparency.
• Lead cross‑functional Joint Project Teams (JPTs) from development to approval, including scenario planning and risk mitigation.
• Develop and maintain compound development strategies, ensuring delivery within budgets and timelines in collaboration with cross‑functional teams.
• Motivate and challenge team members to address issues and meet asset needs.
• Identify potential risks and lead contingency planning; drive problem‑solving within JPTs.

Skills

Leadership

Cross-functional collaboration

Budget management

Strategic thinking

Communication

Project planning

Problem solving

Education

Life Sciences degree

Tools

MS Project

Smartsheet

SharePoint

PowerPoint

Excel

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