{"id":3327052,"url":"https://alion.io/job/fortrea-cra-ii-4","title":"CRA II","company":{"id":3171,"name":"Fortrea","domain":"fortrea.com","url":"https://alion.io/company/fortrea","size_band":"1001-5000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":83,"open_postings":36,"ghost_share":0,"stale_share":0.861,"repost_share":0.028,"time_to_fill_p50_days":20,"computed_at":"2026-11-04T06:34:25Z"}},"role":"Biotech","role_family":"Biotech","seniority":"middle","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Seoul, South Korea"],"countries":["KR"],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":{"min_usd":68000,"max_usd":164000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":136},"experience_years_min":2,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Good Clinical Practice","optional":false},{"name":"Microsoft Office","optional":true},{"name":"Windows","optional":true}],"status":"live","first_seen_at":"2026-10-27T10:31:57Z","employer_posted_date":"2026-10-27","last_verified_at":"2026-11-04T11:42:30Z","board_verified":true,"closed_at":null,"days_open":8,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":8},"description":"*본 포지션은 Core Team 소속으로, 모니터링 경력을 보유한 CRA 분들을 검토하고 있습니다. 포지션 관련 문의는  으로 연락 주세요.\nSummary of Responsibilities:\nSite management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records.\nConducts site monitoring responsibilities for clinical trials according to Fortrea’s Standard Operating Procedures (SOPs), ICH guidelines and GCP; including Pre-study, Site Initiation, Process Monitoring, Routine Monitoring, and Close-out Visits.\nPrepares and implements project plans related to Clinical Monitoring responsibilities.\nEnsures the protection of subjects by verifying that informed consent procedures and protocol requirements are adhered to alongside applicable regulatory requirements.\nSafeguards data integrity by careful source document review, source document verification, query generation, and resolution against established data review guidelines on Fortrea or client data management systems.\nConfirms Site Regulatory documents and applicable eTMF/Sponsor Documents are complete and current throughout the duration of the trial.\nGuarantees that the study Investigational Product inventory and accountability is accurate and that study materials are stored securely and per protocol requirements.\nEnsures adherence to global quality control and CRA performance metrics.\nEnsures audit readiness at site level.\nActs in the project role of a Lead CRA as assigned.\n General On-Site Monitoring Responsibilities:\nEnsure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter subjects/patients into the study. Ensure the protection of study subjects or patients by performing eligibility review, verifying that screening, informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.\nEnsure the integrity of the source data reported by careful source document review. Monitor data for missing or implausible data.\nEnsure study data completeness, accuracy, consistency, and compliance; identify deficiencies, deviations and discrepancies, and initiate corrective action as required.\nEnsure the resources of the Sponsor and Fortrea are spent wisely by performing the required monitoring tasks in an efficient manner, according to SOPs and established guidelines, including managing travel expenses in an economical fashion according to Fortrea travel policy.\nTravel, including air travel, may be required and is an essential function of the job.\nPrepare and submit accurate and timely trip reports.\nIndependently perform eCRF review, 100% source data verification, query generation and resolution against established data review guideline with or without direct supervision, on Fortrea or client data management systems, as assigned by management.\nAssist with the administration of clinical research projects, recruiting investigators (if applicable), collecting investigator documentation and site management.\nUpdate, navigate, and maintain Fortrea or study/Sponsor-specific trial management tools/eClinical systems.\nTrack IP shipments and supplies, as needed.\nTrack and follow-up on serious adverse events as assigned.\nWork closely with the study team, align monitoring to critical study timelines ensuring study deliverables are met.\nPrepare and implement study-specific monitoring plans and site Initiation slides, as assigned.\nAttend investigators’ meetings (if applicable), project team meetings and teleconferences, and others as needed.\nPresent training content for site initiation.\nAssist with training of new employees (e.g., co-monitoring).\nAll other duties as needed or assigned.\nQualifications (Minimum Required):\nUniversity or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). An equivalent amount of experience can be substituted as appropriate.\nThorough understanding of ICH GCP Guidelines and understanding of local regulatory requirements.\nThorough knowledge of monitoring procedures.\nBasic understanding of the clinical trial process.\nFluent in local office language and in English, both written and verbal.\nFortrea may consider relevant and equivalent experience in lieu of educational requirements.\nExperience (Minimum Required):\n External Candidates:\nUniversity or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure). AND\nA minimum of 2 years of Clinical Monitoring experience.\n Internal Candidates:\nInternal candidates with a minimum of 2 years of Clinical Monitoring experience.\nAbility to monitor study sites independently according to monitoring plan, project requirements, SOPs, and ICH GCP guidelines.\nAbility to work with minimal supervision.\nHave an understanding of the Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.\nGood planning, organization, and problem-solving abilities.\nWorks efficiently and effectively in a matrix environment.\nPreferred Qualifications Include:\nThorough working knowledge of Fortrea SOPs for site monitoring.\nOne (1) or more additional years of experience in a related field (i.e., medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.\nPhase I monitoring experience.\nLife Science or Nursing qualification.\nSpecific skills, systems, certifications, and/or licenses preferred.\nPersonal characteristics (leadership, problem solving, interpersonal skills).\nGood attention to detail.\nMethodical approach to work.\nGood understanding of medical and clinical research terminology and clinical research processes.\nAn understanding of the basics of physiology, pharmacology, and medical devices (when applicable).\nGood understanding of the principles of ICH GCP, ISO 14155 (if applicable) and local regulatory requirements.\nGood computer literacy with working knowledge of PCs, Windows and Microsoft Office applications.\nGood oral and written internal and external communication. Strong interpersonal team and organizational skills, personal presentation. The ability to communicate effectively in English.\nFocus on Customer.\nInnovate and Change.\nPursue Scientific and Process Excellence.\nWork with Others.\nAchieve Results.\nAbility to maintain confidentiality of data and information during interactions with staff at all levels and across studies and sponsors.\nDemonstrated ability to conduct clinical operations activities most effectively and efficiently.\nGood analytical and negotiation skills.\nExperience using e-clinical systems [e.g., clinical trial management system (CTMS)].\nFor medical device positions, experience in providing customer service to device end users.\nPhysical Demands/Work Environment:\nMust be able to sit at a computer for long periods of time.\nMust be able to use hands to finger, handle or touch objects, tools or controls, including a computer keyboard, for up to 8 hours per day.\nStandard office and/or home working environment.\nClinical Research Unit and hospital environment (administrative only).\nRisk of eye strain.\nWill involve outside of normal office hours as required by the role.\nTravel Requirement is 60% of the time (traveling to study sites).\nLearn more about our EEO & Accommodations request here.","description_format":"text","description_chars":7486,"description_truncated":false,"requirements":{"experience_years_min":2,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"bachelor","optional":false},"security_clearance":false,"languages":[{"language":"English","level":"All levels","optional":false}]},"benefits":[],"hiring_locations":[],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Services (CRO)"],"lifecycle":[{"event":"open","at":"2026-10-27T10:31:57Z"}],"visa":[],"liveness":{"score":57,"band":"ok","label":"Likely open","p_open":1,"p_active":0.631,"p_room":0.9,"age_days":7,"expected_fill_days":20,"reasons":["conf:0","stale_co","velocity","win:mid","comp:brand"],"computed_at":"2026-11-04T06:34:25Z"},"pay":null,"html_url":"https://alion.io/job/fortrea-cra-ii-4","json_url":"https://alion.io/job/fortrea-cra-ii-4.json","meta":{"generated_at":"2026-11-04T16:23:19Z","cache_seconds":300,"methodology":"https://alion.io/methodology","terms":"https://alion.io/terms","contact":"https://alion.io/contact","api":"https://alion.io/developers","about":"Alion is a live layer of people, companies and AI agents: who they are, whether they are real and active right now, what they do and how to work with them, readable by people and by agents and paid per call.","catalog":"https://alion.io/catalog.json","usage":{"tier":"crawler_verified","counted_by":"address","units_charged":1,"used_today":24970,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-05T00:00:00Z"}},"offers":[{"id":"company.slices","title":"One company in depth, by slice","status":"live","price":{"credits":0.02,"usd":0.002,"plus_per_slice":{"credits":0.05,"usd":0.005}},"unit":"per company, plus each slice with data","note":"the employer in depth","call":{"mcp_tool":"get_company","arguments":{"id":3171},"rest":"https://alion.io/mcp/rest/get_company?id=3171"},"human":"https://alion.io/catalog?offer=company.slices&for=job%2Ffortrea-cra-ii-4"},{"id":"market.stats","title":"A market slice: pay, demand and time to fill","status":"live","price":{"credits":1,"usd":0.1},"unit":"per slice","note":"pay, demand and time to fill for this role and place","call":{"mcp_tool":"market_stats"},"human":"https://alion.io/catalog?offer=market.stats&for=job%2Ffortrea-cra-ii-4"},{"id":"job.search","title":"Open jobs by role, technology, place, pay and visa","status":"live","price":{"credits":0.02,"usd":0.002},"unit":"per posting in a list","note":"similar open postings","call":{"mcp_tool":"search_jobs"},"human":"https://alion.io/catalog?offer=job.search&for=job%2Ffortrea-cra-ii-4"},{"id":"company.verify","title":"Is this company real and active right now","status":"pilot","price":null,"unit":"per company","request":{"url":"https://alion.io/catalog/request","method":"POST","body":"{\"offer\": \"company.verify\", \"for\": \"job/fortrea-cra-ii-4\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Ffortrea-cra-ii-4"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3327052}},{"tool":"search_jobs","arguments":{"company":"fortrea.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3327052},"note":"people open to offers who fit this vacancy"}],"note":"The same data through MCP tools: https://alion.io/mcp/open needs no sign-in (compact searches, postings, people); https://alion.io/mcp with an Alion account has everything. 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