Site Selection Lead at ICON plc

Warsaw, Masovian Voivodeship, Poland -

Full Time

Start Date

Immediate

Expiry Date

02 Sep, 26

Salary

0.0

Posted On

04 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Site Selection, Feasibility Analysis, Clinical Operations, Data Analysis, Stakeholder Management, Cross-functional Coordination, Protocol Requirements, Regulatory Knowledge, Presentation Skills, Clinical Research

Industry

Biotechnology Research

Description

Site Selection Lead - Sofia, Bulgaria - home or office based ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers. We are currently seeking a Site Selection Lead to join our diverse and dynamic team. As a Site Selection Lead at ICON, you will guide strategy and oversight for identifying and recommending investigator sites for assigned studies. You will balance data-driven analysis with operational insight to support reliable and efficient trial delivery. What You Will Be Doing: Leading site selection planning for assigned studies, working closely with feasibility, medical, and operations teams. Analysing data sources, historical performance, and feasibility inputs to inform site lists and recommendations. Coordinating outreach and qualification activities to assess site interest, capabilities, and fit with protocol requirements. Presenting site recommendations and rationale to sponsors and internal stakeholders, incorporating feedback into final decisions. Monitoring early performance to validate selection assumptions and recommending adjustments where needed. Supporting the development of tools, criteria, and processes that enhance consistency and efficiency in site selection. Your Profile: 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. #LI-MK1 Employment with ICON is contingent upon having the legal right to work in the country where the role is based. Rewards & Benefits ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development. Benefits may include: Competitive base salary and performance related incentives Health and wellbeing programmes including medical, dental, and vision coverage where applicable Retirement and pension plans Life assurance and disability coverage Employee assistance programmes and wellbeing resources Learning and development opportunities through structured training and career pathways Benefits may vary depending on role and location. Visit our careers site to read more about the benefits ICON offers. Inclusion and Accessibility ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported. If you require reasonable accommodations during the recruitment process, please let us know or submit a request here. Are you a current ICON Employee? Please click here to apply ICON is an award-winning workplace that enables you to make a difference to patients’ lives by being part of a world-class clinical research organisation that helps deliver new medicines & medical devices that are benefitting patients worldwide. You are also part of a diverse company that cares about our world and is dedicated to conducting business more sustainably and supporting the communities in which we live. If you’re as driven as we are, join us. You’ll be working in a great environment, with some of the brightest and the friendliest people in the sector, and you’ll be helping shape an industry. Didn’t find the role you were looking for? Even if the perfect role isn’t available right now, we’re always excited to connect with talented individuals. Register to our Talent Community to receive updates on roles that align with your career goals.

Responsibilities

Lead the strategy and oversight for identifying and recommending investigator sites for assigned clinical studies. Balance data-driven analysis with operational insights to ensure efficient trial delivery and validate selection assumptions.