Site Selection Lead
On-site · Warsaw, Mazovia, Poland or Sofia, Sofia-Capital, Bulgaria
Job Summary
Site Selection Lead role focused on guiding strategy and oversight for identifying and recommending investigator sites for assigned clinical studies. Lead site selection planning, analyze data sources and feasibility inputs, coordinate outreach and qualification activities, present site recommendations to sponsors, monitor early performance, and contribute to tools and processes that improve consistency and efficiency in site selection. Requires a Bachelor’s degree in life sciences or related field (or equivalent clinical research experience), substantial site selection/feasibility/clinical operations experience, strong analytical and cross-functional coordination abilities, and excellent communication skills. Based in Sofia (BG), Warsaw (PL), or Tbilisi (GE) with role performed on-site or at a company base/hub. ICON emphasizes inclusion, healthcare impact, and opportunities for career development.
Required Qualifications
- Bachelor’s degree in life sciences, healthcare, or a related field, or equivalent clinical research experience
- Substantial experience in site selection, feasibility, or clinical operations
- Strong analytical skills and comfort working with performance data and feasibility outputs
- Good understanding of global site and country dynamics, including regulatory and operational factors
- Excellent communication and presentation skills
- Ability to coordinate cross-functional input and manage multiple studies simultaneously
Desired Qualifications
- Bachelor’s degree in life sciences, healthcare, or a related field, or equivalent clinical research experience
- Substantial experience in site selection, feasibility, or clinical operations
- Strong analytical skills and comfort working with performance data and feasibility outputs
- Good understanding of global site and country dynamics, including regulatory and operational factors
- Excellent communication and presentation skills
- Ability to coordinate cross-functional input and manage multiple studies simultaneously
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