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Global regulatory affairs lead

Salisbury
KalVista Pharmaceuticals
€67,500 a year
Posted: 11h ago
Offer description

A global pharmaceutical company is seeking a Regulatory Manager responsible for managing regulatory submissions and documentation. You will ensure compliance with global marketing authorizations and clinical trial applications while supporting cross-functional teams. Candidates should have a BSc in Pharmacy or a related field, with at least 5 years of pharmaceutical drug development experience, including 2 years in regulatory affairs. Knowledge of global regulations and experience preparing INDs and CTAs is essential. The role offers opportunities to contribute to significant regulatory strategies.
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