Senior Manager, Global Feasibility Lead

CSL's R&D organization is accelerating innovation to deliver greater impact for patients. With a project-led structure and a focus on collaboration, we're building a future-ready team that thrives 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 Senior Manager, Global Feasibility Lead? The job is in our King of Prussia, PA office. This is a hybrid position and is onsite three days a week. You will report to the Senior Director, Head of Feasibility & Patient Engagement; You will be responsible for supporting the strategic planning and execution of global feasibility assessments across clinical development programs. This role ensures that feasibility activities are data-driven, regionally informed, and aligned with the broader clinical and operational strategy.

Responsibilities

• Feasibility Strategy Development: Lead the design and implementation of global feasibility strategies to support protocol optimization and country/site selection.
• Cross-Functional Collaboration: Partner with clinical operations, therapeutic area leads, and external vendors to gather input and align feasibility outputs with study needs.
• Data Analysis & Forecasting: Analyze historical data, epidemiology, and site performance metrics to generate enrollment forecasts and identify potential risks.
• Feasibility Tool Management: Oversee the development and deployment of feasibility tools and templates to ensure consistency and quality across programs.
• Stakeholder Engagement: Facilitate early engagement with investigators and sites to validate feasibility assumptions and support study startup planning. Act as the primary point of contact both internally and externally (e.g., vendors) as applicable for anything study related. Maintain up to date knowledge of the therapeutic area/product candidate(s), clinical practice, competitors, and regulatory considerations. Support audits/inspections and resolutions of findings. Support in the development of new SOPs, guidelines etc and/or participate in working groups about new processes.

Qualifications

• Bachelor's degree or equivalent in life science, nursing, pharmacy, medical laboratory technology, or other health/medical related area preferred. Other degrees and certifications considered if commensurate with related clinical research experience (e.g., diploma or associate degree RN, certified medical technologist).
• 7+ years' relevant clinical research (or related) experience within the pharmaceutical industry.
• A solid understanding of the drug development process, and specifically, each step within the clinical trial process.
• Experience in running feasibility activities for large and/or complex global clinical trials.
• Robust budget forecasting and management experience.
• Thorough knowledge of ICH guidelines/GCP and its applicability to all stages of the clinical development process.