Regulatory Affairs Lead - Phase 1/2 Trials (UK/Hybrid)

A leading drug development organization in Nottingham is looking for a Regulatory Affairs Manager to oversee regulatory activities for early phase clinical trials. This role involves coordinating submissions, maintaining regulatory compliance, and working closely with clients and regulatory authorities. Candidates should have a degree in life sciences and relevant regulatory experience in pharmaceutical settings. This position offers full-time employment with hybrid working options and is essential for ensuring smooth regulatory processes for clinical trials.
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