{"id":3295754,"url":"https://alion.io/job/icon-clinical-study-lead-ctm-ii","title":"Clinical Study Lead (CTM II)","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":81,"open_postings":49,"ghost_share":0,"stale_share":0.98,"repost_share":0,"time_to_fill_p50_days":12,"computed_at":"2026-10-30T05:48:23Z"}},"role":"Biotech","role_family":"Biotech","seniority":"lead","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Blue Bell, United States","Cambridge, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":121576,"max":151970,"currency":"USD","period":"year","gross":null,"usd_annual":151970},"salary_estimate":null,"experience_years_min":5,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-09-18T00:00:00Z","employer_posted_date":"2026-09-18","last_verified_at":"2026-10-30T05:43:18Z","board_verified":true,"closed_at":null,"days_open":42,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":42},"description":"Clinical Trial Manager II (Warren, NJ, Armonk, NY or Cambridge, MA)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\nVendor (e.g., CRO, Biometrics, IXRS, PK/Central Lab, eTMF, Safety) oversight for adherence to budget, timelines and organizational objectives of individual protocols/programs.\n\nDevelops strong vendor and site relationships and ensures continuity of relationships through all phases of the trial.\n\nObtains and maintains in-depth understanding of the study protocol and related procedures in order to contribute strongly to study team knowledge by sharing best practices, making recommendations for continuous improvement and providing training as appropriate/required.\n\nCoordinates & manages various tasks in collaboration with other sponsor roles to achieve site readiness, such as study materials and approval for drug shipping/receipt according to procedure.\n\nPerforms timely review of monitoring reports from CRO and associated deliverables demonstrating sponsor oversight.\n\nPerform periodic reviews of the CRO eTMF/TMF to ensure adherence with standards and compliance with the relevant regulations and guidelines.\n\nWorks with vendors to revise scope of service agreements, budgets, plans and detailed timelines, and ensure that performance expectations are met.\n\nSupports financial management of the study which includes review and approval of site and vendor invoices.\n\nSupports risk Management initiatives\n\nSupports audit/inspection activities as needed.\n\nMaintain clinical trial registry entry/updates, as required.\n\nProvides mentorship/guidance to junior team members or cross-functional colleagues on study processes/study requirements.\n\nYour profile\nUndergraduate degree or its international equivalent preferably in clinical, science, or health related field from an accredited institution; a licensed health-care professional, i.e., registered nurse\n\n5 years of relevant experience including 3 years of experience in clinical trial management\n\nReads, writes and speaks fluent English; fluent in language of host country.\n\nThis is a hybrid role - office based three days per week in Warren, NJ, Armonk, NY or Cambridge, MA\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.\nSalary Range\n$121,576.00-$151,970.00Are you a current ICON Employee? 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