An small but active pharmaceutical team requires a regulatory affairs specialist to engage in a number of regulatory activities on a diverse range of projects, varying in size.

You will have at least 3 years prior experience in this role with a sound comprehension of the pharma development life cycle, ensuring a seamless transition between development phases, for both clinical and non clinical projects. Duties also include managing CTAs and advising a team of 25+ on regulatory requirements.

This is a permanent role with some infrequent on site attendance required.
In addition to your salary you will enjoy a fantastic benefits package coupled with a desirable life/work balance. This is predominantly a fully remote role with some infrequent travel/on site attendance.