Moderna in London is seeking an experienced CMC Regulatory Affairs leader to oversee global regulatory submissions and ensure compliant CMC documentation across vaccine, oncology and rare disease programs. You will lead strategy development for INDs, CTAs, and MAAs, coordinate agency correspondence, and partner with Manufacturing, Quality and Development teams to deliver high-quality filings.
The role requires 10+ years in pharma/biotech, strong EU and ROW regulatory knowledge, and a proactive,
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