{"id":2145786,"url":"https://alion.io/job/cti-senior-clinical-research-associate-level-dependent-on-experience","title":"Senior Clinical Research Associate (level dependent on experience)","company":{"id":23649,"name":"CTI","domain":"cti.ai","url":"https://alion.io/company/cti","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"UltiPro","truth_index":{"grade":"B","score":81,"open_postings":4,"ghost_share":0,"stale_share":0.75,"repost_share":0,"time_to_fill_p50_days":39,"computed_at":"2026-11-05T05:54:30Z"}},"role":"Biotech","role_family":"Biotech","seniority":"senior","employment_type":"full_time","work_mode":"hybrid","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Covington, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":94000,"max_usd":187000,"period":"year","method":"role_seniority_country_remote_cell","sample_n":1015},"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false}],"status":"live","first_seen_at":"2026-10-07T18:32:13Z","employer_posted_date":"2026-10-12","last_verified_at":"2026-11-05T07:55:47Z","board_verified":true,"closed_at":null,"days_open":28,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":28},"description":"What you'll do:\nServe as the main CTI contact for assigned study sites\nConduct site visits (pre-study [PSV], site initiation [SIV], interim monitoring [IMV], and close-out [COV]) and complete site visit deliverables with quality and within given timelines in the Monitoring Plan while adhering to all applicable regulatory requirements, SOPs, and ICH GCP\nAssist with study start-up activities, including feasibility, pre-study activities, and site selection\nCollect, review, and track essential/regulatory documents\nParticipate in and complete all general and study-specific training as required\nParticipate in investigator, client, and project team meetings\nCreate and implement subject enrollment strategies for assigned study sites\nEnsure proper storage, dispensation, and accountability of all Investigational Product (IP) and trial-related materials\nPerform site management activities and provide ongoing updates of site status to the Clinical Project Manager\nConduct remote monitoring and complete the related activities in accordance with study study-specific Monitoring Plan\nUtilize systems and reports to track subject status, subject case report form (CRF) retrieval/source document review (SDV), regulatory documents, and IP\nAssist with project-specific activities as a member of the Project Team\nMay support in the development of CRFs and other study-related documents (subject worksheets, Monitoring Plan, etc.)\nMay support in the translation, customization, and review of Patient Information sheet and Informed Consent, protocol synopsis, and other study-applicable documents as per required procedures\nWhere applicable, provide support to the Regulatory Affairs Study Start-up Team in the preparation orrevision of documentation for submission to Ethics Committee(s), Institutions' Ethics Committees, Regulatory Authorities, Competent Authorities or Institutions Administration Boards, and follow up on the evaluation process until approval is available. Provide regular updates to the Sponsor/ Client\n\nAssist in preparing and coordinating Investigator and client meetings, and attend meetings as necessary\n\nLiaise with Clinical Data Management for data cleaning activities\nIdentify site issues and implement corrective actions or escalate as appropriate\nManage ISF and TMF for all assigned study sites in accordance with SOPs or study-specific Monitoring Plans\nWhere applicable, support in contract negotiation with study sites, Investigator payments, and tracking of site payments\nWhat You'll Bring:\nAt least 1 year of clinical trial monitoring experience or equivalent experience as determined by CTI Management and Human Resources\nBachelor's Degree or higher in an allied health field such as nursing, pharmacy, or health / natural science, or RN with an Associate's Degree, or 3-year Nursing Diploma with at least 2 years clinical nursing experience, or equivalent experience as determined by CTI Management and Human Resources\nPrevious experience in conducting clinical research studies in a hospital setting, a pharmaceutical company, or a CRO\nDemonstrated successful performance in a CRA position with a minimum of 1 year of on-site monitoring experience preferred\nAbout CTI\nCTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visitwww.ctifacts.com\nWhy CTI?\nAdvance Your Career- We support career progression through a structured mentoring program and leadership courses that provide the support needed to grow. We also value ongoing education and training through tuition reimbursement and a dedicated training department.\nJoin an Award-Winning and Valued Team - We have an award-winning unparalleled culture that can be felt by our employees across 60 countries. We support a work-life balance and the importance of time with family by offering generous health benefits and vacation packages, hybrid work from home opportunities, and paid parental leave. We also encourage care for the world around us through our unique CTI Cares program.\nMake a Lasting Impact - We focus on moving medicine forward by working on treatments for chronically and critically-ill patients, who depend on us to bring life-changing therapies to market.\nImportant Note\nIn light of recent increase in hiring scams, if you're selected to move onto the next phase of our hiring process, a member of our team will reach out to you directly from an @ctifacts.comemail address to guide you through our interview process. Please ensure you are applying for jobs directly on our website (www.ctifacts.com) or from our verified LinkedIn page.\nPlease Note\nWe will never communicate directly with you via Microsoft Teams Messaging or by text message\nWe will never ask for your bank account information at any point during the recruitment process\nEqual Opportunity Employer/Protected Veterans/Individuals with Disabilities\nThis employer is required to notify all applicants of their rights pursuant to federal employment laws. 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