About the job
Feasibility Manager – Europe
Chloe O’Shea is proud to partner with a leading global CRO driving innovation in clinical development. We are seeking an experienced Feasibility Informatics Manager to join a high-impact team supporting strategic planning for global clinical trials. This role is open across multiple locations including Bulgaria, Czech Republic, Hungary, Ireland, Latvia, Lithuania, Poland, Portugal, Romania, Serbia, South Africa, Spain, Slovakia, Estonia, the United Kingdom, and Georgia.
This is an exciting opportunity to play a central role in shaping feasibility strategies for key studies across a range of therapeutic areas, leveraging data-driven insights and cross-functional collaboration.
The Role
As a Feasibility Informatics Manager, you will be responsible for leading and managing the feasibility process for global clinical studies at both the pre-award and awarded stages. You will use real-world data, internal performance metrics, and market intelligence to develop robust, data-backed feasibility strategies. This role also involves close collaboration with cross-functional teams and sponsors, ensuring that feasibility insights support both operational strategy and successful bid defense preparation.
This position is ideal for a strategic thinker with a strong analytical mindset and deep understanding of clinical development feasibility planning.
Key Responsibilities
- Drive data-driven feasibility strategies to support proposal development and operational planning.
- Collect and analyze key data from internal sources, sites, and external databases to assess trial viability.
- Prepare strategic feasibility documentation, including site profiles, patient population analysis, competitive landscape, and enrollment risk assessments.
- Collaborate cross-functionally with project managers, patient recruitment, site identification, and therapeutic experts.
- Present and support feasibility strategies in bid defense meetings with sponsors.
- Act as a functional lead for standalone feasibility projects, ensuring timely delivery, stakeholder alignment, and quality reporting.
- Promote process improvement, knowledge sharing, and innovation across feasibility and informatics functions.
- Travel up to 20% (domestic/international) as needed for meetings or presentations.
Requirements
- Master’s degree in life sciences or a related field strongly preferred (Bachelor’s or equivalent considered with relevant experience).
- Minimum of 3 years’ experience in drug development, with at least 2 years in strategic feasibility and data analytics for global clinical trials.
- Strong working knowledge of feasibility data sources, metrics, and analysis techniques.
- Excellent communication and presentation skills, with the ability to engage internal and external stakeholders.
- Experience working across cross-functional teams in a global clinical research environment.
- Fluent in English (spoken and written).
What’s in It for You?
- Competitive compensation and comprehensive benefits tailored to your region.
- Remote-based or home-based flexibility with international scope and collaboration.
- Career progression opportunities within feasibility, operations, and strategic planning.
- Access to industry-leading tools, platforms, and real-world data resources.
- A strong commitment to work-life balance, employee well-being, and ongoing development.
If you’re an experienced feasibility professional looking to step into a high-impact, strategic role within a globally respected CRO, we’d love to hear from you. Apply today and help shape smarter, data-driven decisions in global clinical research.
