PE Global (UK) is seeking a Regulatory Affairs Consultant for the Core Team to oversee regulatory activities focusing on CTAs (Phase I-IV) across multiple Therapeutic Areas, with robust knowledge of regulations and some NZ experience. The role emphasizes project execution, consulting and relationship management, plus potential involvement in business development; exposure to medical devices, GMOs, radiopharmaceuticals, biologics, and labeling for IMPs; knowledge of Quality Documentation and CMC
📌 Regulatory Affairs Consultant: Phase I–IV Trials (Newcastle)
🏢 PE Global (UK)
📍 Newcastle
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