Associate Director, R&D Project Management

CSL is transforming its R&D organization to accelerate innovation and create greater impact for patients. With a streamlined, project-led structure and a focus on collaboration, we're building a future-ready team that excels in dynamic biotech ecosystems. Joining CSL now means being part of an agile team committed to developing therapies that make a meaningful difference worldwide.

Could you be our next Associate Director, Project Management? The job is in our King of Prussia, PA or Maidenhead UK office. This is a hybrid position and is onsite three days a week. You will report to TA Portfolio Delivery Lead.

Position Description:

Responsible for leading the successful operational delivery of global, cross functional R&D projects of strategic importance to CSL's product portfolio.

Main Responsibilities & Accountabilities:

• Work closely with project leader to define strategy and operational tactics


• Responsible for the preparation and management of project budgets, sensitivities, resources, project timelines, project scope and all other project documentation


• Accountable for the accuracy and quality of reports to senior stakeholders


• Lead cross functional development teams through tactical execution of project plans


• Identify, manage and resolve project issues and mitigate risks


• Ensure documentation of key team information, decisions, actions, modifications to scope, resources, timelines and milestones in project management systems is current.


• Identify, evaluate the critical path, scenarios and challenge assumptions to increase robustness of project plans


• Monitor performance vs. plan (budget and timeline)


• Coordinate program updates to Sr. Management


• Provide coaching and mentorship to more junior members of the R&D Global Project Management Department

Qualifications and Experience

• Bachelor degree or equivalent in Science, Engineering, or a related field.


• 10+ years' experience in the biotechnology or pharmaceutical industry


• 5+ years' experience as project manager leading cross-functional project teams in a matrixed, global environment, in-depth knowledge in drug research, development and manufacturing processes


• Demonstrated experience in delivering projects to meet business objectives on time, within budget and with quality.

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