At Blackfield Associates, we are seeking an experienced Associate Director Regulatory Affairs to join our team in Slough. This permanent role requires hybrid working, with a minimum of three days per week spent in the office.
The successful candidate will have a strong background in regulatory affairs, with experience gained in the generics or R&D business. They will be responsible for leading PIP submissions to EMA authorities and CTIS submissions to EMA bodies.
This position offers a salary range of £120,000 - £150,000 per annum, depending on experience. The role also includes a range of benefits, including a pension scheme and life insurance.
In addition to the above, the successful candidate will have a Neurology and injectables portfolio, including due diligence experience. Respiratory experience is also desirable.