Feasibility Lead At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. What You Will Do: Country strategy and feasibility assessment Lead country selection strategy developing data-driven recommendations on country mix, site allocation, and enrollment distribution Oversee CRO completion of design and execution of feasibility assessments including protocol-specific feasibility questionnaires, competitive landscape and trial-density analyses, epidemiology and standard-of-care review, and regulatory and start-up timeline mapping by country. Pressure-test enrollment assumptions by triangulating internal performance data, external intelligence sources, and direct site and investigator input. Site identification and selection Build and maintain a curated, indication-specific site and investigator landscape across North America, Europe, Asia-Pacific, and Latin America, including academic centers, specialty networks, and high-performing private practices. Lead site identification and qualification, coordinating with CRO partners to run pre-study assessments and translating findings into transparent, criteria-based selection recommendations. Track and manage site performance history — enrollment rates, data quality, inspection and audit history, screen-failure patterns, and startup cycle times — and feed that history into future selection decisions. Data, intelligence, and reporting Maintain feasibility metrics and enrollment Present feasibility findings, trade-offs, and recommendations clearly— including where the data is thin and what assumption is carrying the risk. Cross-functional and vendor partnership Serve as the feasibility point of contact for assigned programs, partnering with study teams from concept through first-patient-in. Manage feasibility and site intelligence vendors and CRO feasibility teams — setting scope, holding quality and timeline standards, and reviewing deliverables critically. Partner with Patient Advocacy and Recruitment on patient-finding, referral pathway, and site-support strategies for indications where the eligible population is scarce or highly competed. Your Profile: Bachelor’s degree in life sciences, nursing, public health, or a related field. 5+ years of clinical operations experience in biotech, pharma, or CRO, with extensive experience in country and site feasibility oversight Therapeutic experience: Experience in Immunology highly preferred (dermatology, GI - nice to have) Demonstrated ownership of country selection and/or site selection recommendations for global studies, with the analytical work to support them. Strong quantitative skills — comfortable building enrollment models and country scorecards in Excel and working with trial-landscape and real-world data platforms (e.g., Citeline/Informa, IQVIA, TriNetX, ClinicalTrials.gov, EU CTIS). Working knowledge of ICH GCP, global regulatory and start-up requirements, and country-level submission and approval timelines. Excellent written and verbal communication — able to turn ambiguous data into a clear, defensible recommendation for a senior audience. Ability to manage multiple studies and shifting priorities in a fast-moving, lean organization 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.

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