About this role
Clinical Trial Associate - Central Monitoring (Lachen, CH) at Octapharma. Location: Lachen or Austria or United States. Role: reviewing data, managing queries, escalating issues Requirements: Perform ongoing review of clinical trial data (EDC, IVRS, safety, lab), identify inconsistencies/outliers, manage queries, ensure protocol compliance, and communicate data issues; strong analytical and clinical judgment and attention to detail. English required. Category: Research and Development (R&D) Seniority: Mid Level Tools: EDC, IVRS Commitment: Full Time Workplace: Onsite Languages: English