Site Feasibility Manager

• Lead and execute end‑to‑end in‑house site feasibility activities whilst managing cross‑functional stakeholders across clinical programs.

• Manage creation, sending, tracking and results reporting of the site feasibility questionnaire process for outreach to sites using Veeva Clinical.

• Conduct data analysis to generate comprehensive site feasibility reports and site ranking to present to key stakeholders.

• Conduct analytical data driven feasibility research using clinical trial datasets, real‑world data, and internal resources to inform program and study‑level strategy.

• Assess clinical trial study designs and develop visualizations and data outputs to support evaluation of protocol complexity and patient and site burden.

• Maintain detailed records of work and internal databases

• Engage with Program Feasibility Leads to support scenario modelling for impact to clinical trial operational designs

• Bachelor’s degree required, Masters or PhD in associated drug development field preferred
• 4+ years of biotech, pharmaceutical or CRO clinical operations experience and/or early engagement/site feasibility management
• Excellent decision‑making, communication, and presentation skills
• Previous experience conducting site feasibility activities in Veeva Clinical or similar site feasibility platform preferred
• Demonstrated success in working cross‑functionally in a global matrix organization
• High proficiency in analysis and data visualization skills/ tools, essential experience with Excel, VBA/macros experience is preferred.
• Additional experience with visualization tools such Power Bi, Spotfire, Tableau, statistical analysis/programming, etc.

• Clinical Operations
• Site Feasibility Activities
• Statistical Analysis
• Excel
• VBA
• Power BI
• Spotfire
• Tableau
• Data Reporting
• Scenario Modelling

• Decision‑Making
• Communication
• Presentation Skills

• Bachelor’s Degree
• Master’s Degree
• PhD