Associate Director, Regulatory Affairs
Salisbury
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Blackfield Associates in the United Kingdom is expanding its European Regulatory Affairs team, seeking a Senior Regulatory Affairs Manager to lead EMA Centralised Procedure MAAs from submission to approval and manage MHRA submissions for a portfolio of innovative products.
The role requires 5–10 years of Regulatory Affairs experience, a Pharmacy or Life Sciences degree, and the ability to work in a hybrid setup from Slough, with mentoring responsibilities for junior team members.
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Salisbury
Join to apply for the Associate Director, Regulatory Affairs role at KalVista Pharmaceuticals, Inc.
Cambridge, Cambridgeshire
Are you ready to shape European regulatory strategy that accelerates innovative oncology medicines to patients and secures the strongest possible…
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