{"id":3265114,"url":"https://alion.io/job/icon-clinical-trial-liaison-3","title":"Clinical Trial Liaison","company":{"id":5677,"name":"ICON","domain":"iconplc.com","url":"https://alion.io/company/icon","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"A","score":85,"open_postings":58,"ghost_share":0,"stale_share":0.81,"repost_share":0,"time_to_fill_p50_days":20,"computed_at":"2026-11-06T05:58:05Z"}},"role":"Sales","role_family":"Sales","seniority":"senior","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"board_field","remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["United States"],"countries":["US"],"hiring_countries":["US"],"hiring_countries_total":1,"salary":null,"salary_estimate":{"min_usd":84000,"max_usd":164000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":2094},"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-10-01T00:00:00Z","employer_posted_date":"2026-10-01","last_verified_at":"2026-11-06T06:27:57Z","board_verified":true,"closed_at":null,"days_open":36,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":36},"description":"Clinical Trial Liaison - NeurologyAt ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.\nAs 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.\nAs a Clinical Trial Liaison at ICON, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This is an FSP dedicated position supporting Neurology trials.\nWhat you will do:\nClinical Investigator Management\nAccountable for the full spectrum of investigator engagement from identification and qualification through enrollment, and support database lock, and study closeout \nServe as a clinical trial scientific ambassador, ensuring investigators deeply understand protocol intent, scientific rationale, and patient eligibility requirements \nDevelop and sustain strategic, high-trust relationships with investigators that span trials and therapeutic areas \nInfluence enrollment by co-creating tailored recruitment strategies aligned with site capabilities, patient population realities, and study objectives \nProactively find opportunities to reach new patients, accelerate enrollment and increase impact at priority sites, including for example, novel site models, community-based research initiatives etc \nCapture and elevate critical insights from sites to optimize feasibility, protocol design, and study conduct \nClinical Trial Management\nLead site-level strategy and risk planning to ensure strong and predictable enrollment and data delivery \nLeverage performance metrics to anticipate issues, intervene decisively, and maintain momentum toward clinical milestones \nDrive inspection readiness as a continuous discipline across sites \nCollaborate across functions and with vendor partners to resolve operational barriers, ensuring delivery with speed and quality \nMaintain advanced understanding of local treatment paradigms and standard of care to influence strategic country/site selection and protocol localization \nProvide oversight and quality assurance for vendor monitoring, escalating risks proactively \nWhere applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations \nBusiness Management and Engagement\nCultivate a portfolio of strategically aligned, high-impact investigators who consistently prioritize client trials \nEnable an exceptional investigator experience by being a responsive, knowledgeable, and valued scientific partner \nCollaborate cross-functionally (e.g., Medical, Clinical, Study Delivery) to align on trial and site priorities, troubleshooting challenges with urgency and creativity \nConduct data-informed site prospecting and prioritization, contributing to trial competitiveness and regional strategic execution \nMaintain scientific fluency and therapeutic expertise to lead meaningful, solutions-focused discussions with site personnel \nAct as a key liaison between field teams, vendors, and investigators, ensuring alignment, shared purpose, and continuous knowledge transfer \nPartner closely with field team colleagues to elevate the investigator and site experience, ensuring seamless collaboration and improving enrollment outcomes and Investigator relationships \n You are:\nBachelor’s degree or equivalent; strong preference for scientific, clinical, or health-related fields \nMinimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites \nOpen to up to 60-80% travel during peak times (travel will vary)\nIdeal if they have experience in Neurodegen/Alzheimer's\nEmployment with ICON is contingent upon having the legal right to work in the country where the role is based.\nRewards & Benefits\nICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.\nBenefits may include:\nCompetitive base salary and performance related incentives\nHealth and wellbeing programmes including medical, dental, and vision coverage where applicable\nRetirement and pension plans\nLife assurance and disability coverage\nEmployee assistance programmes and wellbeing resources\nLearning and development opportunities through structured training and career pathways\nBenefits may vary depending on role and location.\nVisit our careers site to read more about the benefits ICON offers.\nInclusion and Accessibility\nICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.\nIf you require reasonable accommodations during the recruitment process, please let us know or submit a request here.\nAre you a current ICON Employee? 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