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Own regulatory strategy and submissions for an early clinical programme, working with the MHRA and EMA.
What you’ll do
- Plan and write clinical trial applications and amendments
- Act as the main contact with regulators
- Advise project teams on regulatory risk
What you’ll need
- Regulatory affairs experience in clinical development
- Track record of UK and EU submissions
- Life science degree, with a higher degree an advantage
About the employer
Clinical stage biotech in Cambridgeshire. We share the employer’s name when we speak to you about the role. Questions first? Call us on 07884 493960 and quote NLS-1035.