Regulatory Affairs Manager (Licensed Pharmacists)

We are partnering with a leading academic and clinical research environment to appoint a Regulatory Affairs Manager who is also a licensed pharmacist (essential requirement).

This is a unique opportunity for a pharmacist looking to transition into or deepen their career in regulatory affairs, working at the intersection of clinical trials, manufacturing, and translational science. You’ll play a key role in bringing innovative therapies from early research into clinical development.

Key Responsibilities

• Liaise with manufacturing partners (CDMOs) to support product development and ensure regulatory and GMP compliance
• Act as a key interface, negotiating with pharmaceutical and biotech partners on behalf of UCL-sponsored trials
• Support the Head of Clinical Trials Operations in developing policies, SOPs, and training workshops for complex studies
• Collaborate with scientists, clinicians, and the Translational Research Office to advance preclinical research into early-phase clinical trials
• Provide GMP/QA oversight, including due diligence and auditing external manufacturing vendors
• Work closely with senior pharmacy leadership on IMP (Investigational Medicinal Product) handling requirements
• Review preclinical data and contribute to translational strategy and clinical development pathways
• Support the preparation and review of key regulatory documents including Investigator’s Brochures (IBs) and IMPDs