{"id":3015992,"url":"https://alion.io/job/fortrea-clinical-data-spec-coordinator","title":"Clinical data Spec- Coordinator","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":"A","score":85,"open_postings":43,"ghost_share":0,"stale_share":0.767,"repost_share":0.023,"time_to_fill_p50_days":20,"computed_at":"2026-11-08T05:47:12Z"}},"role":"Administrative","role_family":"Administrative","seniority":"junior","employment_type":"full_time","work_mode":"remote","remote_scope":"stated_countries","remote_scope_basis":"posting_text","remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["San José, Costa Rica"],"countries":["CR"],"hiring_countries":["CR"],"hiring_countries_total":1,"salary":null,"salary_estimate":{"min_usd":18500,"max_usd":34000,"period":"year","method":"global_role_cell_scaled_by_country","sample_n":5657},"experience_years_min":1,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[{"name":"CDISC","optional":false},{"name":"Good Clinical Practice","optional":false},{"name":"Microsoft Office","optional":false}],"status":"live","first_seen_at":"2026-07-06T00:00:00Z","employer_posted_date":"2026-07-06","last_verified_at":"2026-11-08T17:07:29Z","board_verified":true,"closed_at":null,"days_open":125,"trust":{"level":"stale","repost_count":0,"flags":["stale"],"days_open":125},"description":"Clinical Data Specialist - Coordinator\nLocation: Costa Rica (candidates must be based in Costa Rica)\nDepartment: Clinical Data Management\nAdvance clinical research through data precision\nWe are looking for a detail-oriented and collaborative Clinical Data Specialist - Coordinator to join our growing Clinical Data Management team.\nIn this role, you will support the integrity, quality, and timely delivery of clinical trial data from external sources, contributing directly to studies that improve patient outcomes worldwide.\nWhat You’ll Do\nSupport the acquisition, review, and integration of external clinical trial data throughout the study lifecycle\nCoordinate with internal teams and external vendors to ensure accurate and timely data delivery\nPerform data quality checks and assist in resolving discrepancies\nContribute to study deliverables under the guidance of experienced data leads\nParticipate in study-related activities, including meetings and task coordination\nHelp prioritize tasks, manage timelines, and escalate issues when needed\nWork across multiple studies with diverse data sources and therapeutic areas\nWhat You Bring\nBachelor’s degree in Life Sciences, Health Sciences, Technology, or related field (or equivalent experience)\nApproximately 1+ year of experience in clinical research or drug development\nBasic understanding of clinical trials, ICH-GCP, and data quality principles\nFamiliarity or interest in clinical data standards (e.g., CDISC, SDTM, ADaM)\nStrong attention to detail and problem-solving skills\nEffective communication and collaboration abilities\nAbility to manage multiple priorities in a dynamic environment\nProficiency in Microsoft Office tools\nWhy Join Us?\n Work on global clinical trials across diverse therapeutic areas\n Build expertise in clinical data and external data integration\n Collaborate with cross-functional and international teams\n Grow your career in a supportive and structured environment\nImportant Requirement\nCandidates must be currently based in Costa Rica\nWho You Are\nYou are detail-driven, proactive, and eager to build a career in Clinical Data Management. 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