{"id":2469894,"url":"https://alion.io/job/fortrea-clinical-trial-manager","title":"Clinical Trial Manager","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":16,"computed_at":"2026-11-01T06:10:25Z"}},"role":"Biotech","role_family":"Biotech","seniority":"middle","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":["Durham, United States","Canada"],"countries":["US","CA"],"hiring_countries":["US"],"hiring_countries_total":1,"salary":{"min":76000,"max":148000,"currency":"USD","period":"year","gross":null,"usd_annual":148000},"salary_estimate":null,"experience_years_min":4,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"GCP","optional":false},{"name":"Medidata Rave","optional":false},{"name":"Microsoft Office","optional":false},{"name":"Veeva","optional":false}],"status":"live","first_seen_at":"2026-09-25T00:00:00Z","employer_posted_date":"2026-10-21","last_verified_at":"2026-11-01T13:34:18Z","board_verified":true,"closed_at":null,"days_open":37,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":37},"description":"Fortrea is seeking Clinical Trial Managers to join our team! We are seeking experienced CTLs with 3+ years of experience. Remote US or Canadian based.\nJob Overview:\nThe Clinical Trial Manager has ownership in the clinical delivery and operational oversight of clinical research trials. This role collaborates with project managers and other functional leads to deliver clinical and start-up activities within budget and contract, ensuring quality, compliance and meeting country-specific commitments.\nThe role generally works under the direction of a (Senior) Clinical Trial Manager, however, may also work independently at a lower complexity study.\nSummary of Responsibilities:\nEnd-to-end oversight of start-up and clinical responsibilities-from site identification through to database lock-through proactive management of project scope, timelines, milestones, and budget.\n\nEnsure start-up and clinical project plans address identified risks while adhering to professional standards, SOPs, client, and regulatory requirements.\n\nProactively identify and address start-up and clinical project, financial, and quality risks by applying comprehensive risk management strategies and ensuring compliance, including tracking within applicable systems.\n\nResponsible for financial aspects of clinical and start-up activities, including revenue forecasting, adherence to contracted scope, and oversight of scope modifications.\n\nEnsure project team awareness and tracking of Key Project Indicators (KPI) for any client-specific start-up and clinical metrics.\n\nEnsure and plans for start-up and clinical resources with accurate projections for the resourcing teams.\n\nDevelop and implement the site activation and recruitment strategy in collaboration with project teams.\n\nLead and oversee site identification and site selection.\n\nOversight of Informed Consent Form development and translations.\n\nOversight of essential document creation and collection, including insurance.\n\nOversight of the development, negotiation, and execution of Clinical Trial Agreements (CTA), including site budgets.\n\nLead the end-to-end process of regulatory/ethics committee submissions, approvals, and tracking.\n\nEnsure clinical and ancillary supplies -including import/export logistics and supply destruction processes- are in place as applicable.\n\nManage operational aspects to support subject recruitment and retention, patient safety, vendor performance, and the monitoring visit strategy.\n\nProactive planning for monitoring activities to ensure data integrity, patient safety and endpoint protection.\n\nEnsure inspection-readiness through quality oversight of TMF, monitoring reports, protocol deviations and issue management.\n\nOversight and approval of site payments, including payment reconciliation.\n\nFoster effective communication and collaboration with clients and cross-functional project teams in a global and multicultural environment.\n\nAbility to lead client-facing calls to communicate project status updates and demonstrate operational control of start-up and clinical deliverables.\n\nSupport new business with active participation in pre-award preparation as required.\n\nProvide feedback on team members as needed to respective line managers.\n\nAll other duties as needed or assigned.\n\nQualifications (Minimum Required):\nUniversity/college degree (life science preferred) or certification in a related allied health profession (nursing, medical, or laboratory technology) from an appropriately accredited institution.\n\nFortrea may consider relevant and equivalent experience in lieu of educational requirements.\n\nFluent in English, both written and verbal\n\nExperience (Minimum Required):\nFour or more years of relevant clinical research experience in pharmaceutical, CRO, or health care setting will be considered.\n\nPrevious SSU and Clinical Trial Lead experience\n\nComprehensive knowledge of GCP, ICH, and regulatory guidelines.\n\nProficiency in Microsoft Office and familiarity with EDC, CTMS, eTMF, and vendor platforms (e.g. Veeva Vault, Medidata).\n\nEffective leadership in remote and global environment.\n\nStrong communication, planning, and organizational abilities.\n\nProven team motivational skills.\n\nProficiency in balancing concurrent tasks within time-sensitive environments.\n\nFinancial awareness and use of tracking systems/tools.\n\nDemonstrated independent problem-solving and risk management mindset.\n\nDemonstrated professional client interaction and presentation skills, with ability to work independently and collaboratively.\n\nIn this role, employees will leverage their existing experience and skills to assume additional responsibilities within the broader role. These will be aligned with operational requirements and internal training, without altering the fundamental nature or classification of the position.\nPreferred Qualifications Include:\nMaster’s or other advanced degree.\n\nPMP certification or equivalent.\n\nPhysical Demands / Work Environment:\nRemote-based work required with possible office presence depending on location.\n\nTravel requirements: up to 20% (global - primarily domestic and international)\n\nPay Range: $76,000 - 148,000 USD annually\nLearn more about our EEO & Accommodations request here.","description_format":"text","description_chars":5205,"description_truncated":false,"requirements":{"experience_years_min":4,"management_years_min":null,"team_size_min":null,"manages_managers":false,"education":{"level":"master","optional":false},"security_clearance":false,"languages":[{"language":"English","level":"Advanced (C1)","optional":false}]},"benefits":[],"hiring_locations":[{"name":"United States","iso":"US","kind":"country"}],"hiring_excludes":[],"relocation_offered":false,"industries":["Clinical Trial Services (CRO)"],"lifecycle":[{"event":"open","at":"2026-10-13T19:33:28Z"},{"event":"close","at":"2026-10-21T13:27:52Z"},{"event":"reopen","at":"2026-10-21T19:42:46Z"}],"visa":[{"country":"US","licensed_sponsor":true,"evidence":"H-1B filings in 12 months: 23 · green card filings: 9","filings_12m":23,"filings_prev_12m":17,"green_card_filings_12m":9,"median_offered_wage_usd":126094,"route":null,"cap_exempt":false,"checked_at":"2026-10-29T16:27:21+00:00","sources":["US Department of Labor: LCA disclosure data (H-1B, H-1B1, E-3)","US Department of Labor: PERM disclosure data (green cards)"],"filings_for_role_12m":0}],"liveness":{"score":15,"band":"cold","label":"Long shot","p_open":1,"p_active":0.419,"p_room":0.35,"age_days":37,"expected_fill_days":16,"reasons":["conf:3","stale_co","velocity","win:tail","comp:brand"],"computed_at":"2026-11-01T06:10:25Z"},"pay":{"stated_usd_annual":148000,"is_top_pay":true},"html_url":"https://alion.io/job/fortrea-clinical-trial-manager","json_url":"https://alion.io/job/fortrea-clinical-trial-manager.json","meta":{"generated_at":"2026-11-01T22:08:14Z","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":33797,"day_limit":null,"remaining_today":null,"minute_limit":300,"resets_at":"2026-11-02T00:00:00Z"}},"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-clinical-trial-manager"},{"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-clinical-trial-manager"},{"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-clinical-trial-manager"},{"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-clinical-trial-manager\", \"note\": \"what you need it for\"}"},"human":"https://alion.io/catalog?offer=company.verify&for=job%2Ffortrea-clinical-trial-manager"}],"agent":{"mcp":"https://alion.io/mcp/jobs","mcp_open":"https://alion.io/mcp/open","next":[{"tool":"get_job","arguments":{"id":2469894}},{"tool":"search_jobs","arguments":{"company":"fortrea.com","detail":"compact"}},{"tool":"match_people","arguments":{"job_id":2469894},"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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