{"id":1995644,"url":"https://alion.io/job/humaneva-group-senior-clinical-data-coordinator","title":"Senior Clinical Data Coordinator","company":{"id":3902831,"name":"Humaneva Group","domain":"humaneva.com","url":"https://alion.io/company/humaneva-group","size_band":"51-200","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"BambooHR","truth_index":null},"role":"Administrative","role_family":"Administrative","seniority":"senior","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"inferred","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}],"status":"live","first_seen_at":"2026-10-07T08:43:34Z","employer_posted_date":"2026-10-07","last_verified_at":"2026-10-13T22:36:16Z","board_verified":true,"closed_at":null,"days_open":6,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":6},"description":"Key Responsibilities:\nCoordinate Endpoint Adjudication Committee (EAC) activities, including case initiation, review, voting, and decision form distribution.\nReview and reconcile clinical trial data for completeness, accuracy, and protocol compliance.\nManage adjudication case packets and ensure timely collection and submission of source documents.\nGenerate, track, and resolve clinical data and adjudication-related queries.\nPrepare and maintain adjudication documents, forms, reports, listings, and study materials.\nDevelop and maintain CRFs, data management plans, tracking logs, and study documentation.\nPerform data review, quality control, and data cleaning to ensure data integrity.\nMonitor case status, study metrics, and operational performance reporting.\nServe as a liaison between sponsors, sites, committee members, vendors, and external stakeholders.\nCoordinate data transfers and exchanges with vendors, laboratories, and imaging review partners.\nSupport the development and implementation of EAC processes, workflows, and operational tools.\nEnsure compliance with ICH-GCP, regulatory requirements, study protocols, and SOPs.\nParticipate in study meetings, training activities, and cross-functional collaborations.\nEducation, Skill & Experience:\nMinimum Master's/Pharm D degree in any discipline. 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