You will support the ClinDev EU team with audits and regulatory inspections by preparing documentation, tracking CAPAs, and reviewing trial-related manuals and plans to communicate quality requirements. * You possess in-depth knowledge of ICH E6(R2/R3), EU CTR, EMA/FDA inspection behaviors, SOP governance, and trial-specific oversight plans, and you are skilled at prioritizing multiple tasks to meet timelines. * 30 days of vacation, discounted ticket to Germany, (e)-bike leasing, capital-forming benefits, company pension plan, disability insurance, canteen, and much more.
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