ICON
Feasibility Lead
Pennsylvania · North Carolina · Texas
Get past the screening software and onto a recruiter's desk
hirly rewrites your resume for this job — matching the keywords and skills in the posting, moving your most relevant experience to the top, and writing a cover letter to fit. About 30 seconds.
- Keywords matched to this posting
- Fit score before you apply
- Cover letter included
Apply from your AI assistant
Connect hirly to Claude and ask it to apply to this job. hirly tailors your resume, fills the employer’s form and asks before sending. ChatGPT: manual setup today.
Some employer sites stop an application at a CAPTCHA or sign-in and hand it back with a link. Applying needs a paid plan. Works with any assistant that supports MCP.
hirly's read of this role
- Seniority
- Lead / management
- Country
- US
- Work mode
- On-site / unstated
- First seen by hirly
- 9 Oct 2026
Derived automatically from the posting. Upload your resume above to see how the role scores against it.
the posting
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
Listed on hirly, a job board. hirly is not the employer: ICON is hiring for this role.
Similar jobs
Browse similar roles
Want this one?
Upload your resume and hirly rewrites it for this job and writes the cover letter — in about thirty seconds, before you sign up.
Tailor my resume for this job