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Senior Manager, Global Feasibility Lead

Job in King of Prussia, Montgomery County, Pennsylvania, 19406, USA
Listing for: CSL Plasma Inc.
Full Time position
Listed on 2026-02-01
Job specializations:
  • Management
    Healthcare Management, Data Science Manager
Salary/Wage Range or Industry Benchmark: 120000 - 150000 USD Yearly USD 120000.00 150000.00 YEAR
Job Description & How to Apply Below
Senior Manager, Global Feasibility Lead page is loaded## Senior Manager, Global Feasibility Lead locations:
Americas, US-PA, King of Prussia, CSL Behring time type:
Full time posted on:
Offerta pubblicata ierijob requisition :
R-268457

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.

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.

Operating within a matrixed and cross-functional environment, you will collaborates with therapeutic area leads, clinical operations teams, and external service providers to deliver feasibility insights that inform country and site selection, enrollment forecasting, and risk mitigation strategies. The role contributes to the development and implementation of feasibility tools, monitors feasibility data integrity, and ensures timely delivery of feasibility outputs to support protocol finalization and study startup.

This position plays an important role in early engagement with investigators and sites, helping shape the feasibility narrative and supporting the operational design of clinical trials. You will be expected to identify potential feasibility risks, recommend mitigation strategies, and escalate issues as appropriate to enable successful trial execution.
** 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 inworking 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#LI-HYBRID## ## ##
** About CSL Behring
** CSL Behring is a global biotherapeutics leader driven by our promise to save lives. Focused on serving patients’ needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the…
Position Requirements
10+ Years work experience
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