{"id":3542996,"url":"https://alion.io/job/fortrea-cra-i-4","title":"CRA I","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":82,"open_postings":32,"ghost_share":0,"stale_share":0.938,"repost_share":0,"time_to_fill_p50_days":17,"computed_at":"2026-11-02T06:13:15Z"}},"role":"Biotech","role_family":"Biotech","seniority":"junior","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":["Buenos Aires, Argentina"],"countries":["AR"],"hiring_countries":["AR"],"hiring_countries_total":1,"salary":null,"salary_estimate":{"min_usd":33000,"max_usd":84000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":183},"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"Good Clinical Practice","optional":true},{"name":"Microsoft Office","optional":true},{"name":"Windows","optional":true}],"status":"live","first_seen_at":"2026-10-30T19:50:09Z","employer_posted_date":"2026-10-30","last_verified_at":"2026-11-03T02:14:10Z","board_verified":true,"closed_at":null,"days_open":3,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":3},"description":"Job Overview:\nSite monitoring and site management responsibility for clinical studies according to Company, and/or Sponsor, Standard Operating Procedures, and Regulatory Guidelines. Assures the implementation of project plans, as assigned.\nSummary of Responsibilities:\nResponsible for all aspects of study site monitoring including routine monitoring and closeout of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned.\nResponsible for all aspects of site management as prescribed in the project plans.\nGeneral On-Site Monitoring Responsibilities.\nEnsure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study.\nEnsure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements.\nEnsure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document review.\nMonitor data for missing or implausible data.\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.\nEnsure audit readiness at the site level.\nTravel, including air travel, may be required and is an essential function of the job.\nPrepare accurate and timely trip reports.\nInteract with internal work groups to evaluate needs, resources, and timelines.\nAct as contact for clinical trial supplies and other suppliers (vendors) as assigned.\nResponsible for all aspects of registry management as prescribed in the project plans.\nUndertake feasibility work when requested.\nParticipate in and follow-up on Quality Control Visits (QC) when requested.\nRecruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor as assigned 18) Assist Senior CRA with managing investigator site budgets.\nTrack and follow-up on Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs.\nIndependently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management.\nAssist with training, mentoring and development of new employees, e.g., co-monitoring.\nCoordinate designated clinical projects as a Local Project Coordinator (with supervision, if applicable), and may act as a local client contact as assigned.\nPerform other duties as assigned by management.\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.\nFortrea may consider relevant and equivalent experience in lieu of educational requirements.\nBasic knowledge of Regulatory Guidelines.\nBasic understanding of the clinical trial process.\nFluent in local office language and in English, both written and verbal.\nExperience (Minimum Required):\nSix (6) months experience in a related role (e.g., site management, in-house CRA, study coordinator, research nurse, etc.).\nBasic understanding of Regulatory Guidelines.\nAbility to work within a project team.\nGood planning, organization, and problem-solving skills.\nGood computer skills with good working knowledge of a range of computer packages.\nWorks efficiently and effectively in a matrix environment.\nValid Driver's License.\nPreferred Qualifications Include:\nOne (1) or more year's additional experience in a related field (i.e., medical, clinical, pharmaceutical, laboratory, research, data analysis, data management or technical writing) is preferred.\n6 months on site monitoring experience.\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.\nAttention to detail.\nMethodical approach to work.\nUnderstanding of medical and clinical research terminology and clinical research processes.\nAn understanding of the basics of physiology, pharmacology, and medical devices (when applicable).\nUnderstanding of the principles of ICH GCP, ISO 14155 (if applicable) and 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.\nExperience using a clinical trial management system (CTMS).\nFor medical device positions, experience in providing customer service to device end users.\nLearn more about our EEO & Accommodations request here.","description_format":"text","description_chars":5180,"description_truncated":false,"requirements":{"experience_years_min":1,"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":[{"name":"Argentina","iso":"AR","kind":"country"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Services (CRO)"],"lifecycle":[{"event":"open","at":"2026-10-30T19:50:09Z"}],"visa":[],"liveness":{"score":70,"band":"hot","label":"Hiring now","p_open":1,"p_active":0.695,"p_room":1,"age_days":2,"expected_fill_days":17,"reasons":["conf:1","stale_co","wave","velocity","win:early","comp:junior,brand"],"computed_at":"2026-11-02T06:13:15Z"},"pay":null,"html_url":"https://alion.io/job/fortrea-cra-i-4","json_url":"https://alion.io/job/fortrea-cra-i-4.json","meta":{"generated_at":"2026-11-03T03:18:36Z","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":4352,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-04T00:00:00Z"}},"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-i-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-i-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-i-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-i-4\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Ffortrea-cra-i-4"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":3542996}},{"tool":"search_jobs","arguments":{"company":"fortrea.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":3542996},"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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