{"id":1464993,"url":"https://alion.io/job/linical-clinical-research-associate-ii-spain","title":"Clinical Research Associate II - Spain","company":{"id":1916604,"name":"Linical","domain":"linical.com","url":"https://alion.io/company/linical","size_band":"501-1000","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Teamtailor","truth_index":null},"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":"explicit","locations":[],"countries":[],"hiring_countries":[],"hiring_countries_total":0,"salary":null,"salary_estimate":null,"experience_years_min":4,"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":"2026-09-25T11:01:00Z","employer_posted_date":"2026-09-25","last_verified_at":"2026-11-05T02:59:40Z","board_verified":true,"closed_at":null,"days_open":40,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":40},"description":"Are you an experienced Clinical Research Associate looking to join a dynamic and growing clinical research organisation?\nWe are seeking a CRA II to manage investigative sites across Spain, ensuring clinical trials are conducted in accordance with study protocols, ICH-GCP, and applicable regulatory requirements.\nKey Responsibilities\nConduct site qualification, initiation, monitoring, and close-out visits.\n\nEnsure patient safety, data integrity, and protocol compliance.\n\nPerform source data verification and review study documentation.\n\nManage site relationships and provide ongoing support to investigators and study staff.\n\nAssist with ethics committee and regulatory submissions where required.\n\nMonitor investigational product accountability and site performance.\n\nMaintain Trial Master File (TMF) documentation and support query resolution.\n\nCollaborate with cross-functional study teams to ensure successful trial delivery.\n\nAbout You\nLife Sciences degree or equivalent experience, plus recognized CRA training.\n\nMinimum 4 years' clinical research experience.\n\nMinimum 2 years' monitoring experience as a CRA.\n\nStrong knowledge of ICH-GCP, clinical trial regulations, and site management.\n\nFluent in Spanish and English languages, Portuguese is desirable\n\nExcellent communication, organisation, and problem-solving skills.\n\nAbility to work independently and manage multiple priorities.\n\nValid driver's license and willingness to travel up to 75%.\n\nWhat We Offer\nHome-based flexibility.\n\nOpportunity to work on international clinical trials.\n\nCollaborative and supportive team environment.\n\nCompetitive salary and benefits 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