{"id":3251383,"url":"https://alion.io/job/icon-clinical-research-associate-14","title":"Clinical Research Associate","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":"B","score":80,"open_postings":5,"ghost_share":0,"stale_share":1,"repost_share":0,"time_to_fill_p50_days":5,"computed_at":"2026-10-26T05:57:25Z"}},"role":"Biotech","role_family":"Biotech","seniority":"junior","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"posting_text","remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Blue Bell, United States"],"countries":["US"],"hiring_countries":["US"],"hiring_countries_total":1,"salary":null,"salary_estimate":null,"experience_years_min":2,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Good Clinical Practice","optional":false}],"status":"live","first_seen_at":"2026-10-13T00:00:00Z","employer_posted_date":"2026-10-13","last_verified_at":"2026-10-26T06:09:02Z","board_verified":true,"closed_at":null,"days_open":13,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":13},"description":"Clinical Research Associate - Early Development Multi Therapeutic - Regional (major hubs)At 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.\nWhat you will be doing:\nServe as the primary point of contact between investigation sites and the sponsor for early development multi therapeutic clinical trials.\n\nConduct all types of site visits, including selection, initiation, routine monitoring, and close-out\n\nEnsure site compliance with ICH-GCP, SOPs, and regulations\n\nMaintain up-to-date documentation in CTMS and eTMF systems\n\nSupport and track site staff training and maintain compliance records\n\nMonitor patient safety, ensuring timely and accurate AE/SAE/PQC reporting\n\nSupport subject recruitment and retention efforts at the site level\n\nOversee drug accountability and ensure proper storage, return, or destruction\n\nResolve data queries and drive timely, high-quality data entry\n\nDocument site progress and escalate risks or issues to the clinical team\n\nAssist in tracking site budgets and ensuring timely site payments (as applicable)\n\nCollaborate with cross-functional partners including CTAs, LTMs, and CTMs\n\nYou are:\nA graduate with a Bachelor’s degree in Life Sciences or equivalent, or a qualified RN\n\nEligible to work in United States without visa sponsorship\n\nA clinical research professional with 2+ years of on-site monitoring experience in the pharmaceutical or CRO industry\n\nExperienced monitoring early development Phase I/II clinical studies, across multiple therapeutic areas\n\nProficient in ICH-GCP, local regulatory requirements, and clinical systems like CTMS and eTMF\n\nA clear communicator, problem-solver, and collaborative team player\n\nWilling and able to travel up to 60% for on-site monitoring visits; preference given to candidates residing near major HUB airports to support efficient regional travel.\n\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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