Project Manager - Regulatory Affairs

Our client is looking for a passionate and experienced project manager with commercial experience working within the pharmaceutical industry specifically within Regulatory Affairs.

Key responsibilities include

Project management for global regulatory activities and submissions for all Therapeutic Areas.
Participates in meetings with the regulatory teams to coordinate, prioritise, plan, and track submissions for the regulatory liaisons.
Liaise with affiliates with consideration given to the broader impact of decisions or issues arising from this interaction
Works closely with cross-functional submissions teams to ensure that submissions are prepared in accordance with agreed time lines
Acts as a primary contact for regulatory project management questions on one or more products or indications across a number of countries

experience required
Experience within Regulated Industry preferred
3+ years of Project Management experience preferred
Degree in a scientific field is preferred

Allegis Group Limited and Aston Carter Limited operate Employment Businesses and Agencies and are companies within the Allegis Group Inc. group of companies, the fourth largest staffing company in the world, (collectively referred to as the "Allegis Group"). TEKsystems and Aerotek are divisions of Allegis Group Limited. Applicant data will be treated in accordance with the Allegis Group's Privacy Notice. By submitting personal data to any company or division within the Allegis Group, the applicant is providing explicit consent to the use of such data by the Allegis Group and to the transfer of such data to and from the Allegis Group companies within the UK, Europe and outside the European Economic Area in connection with the fulfilment of the applicant's voluntary requests, and the fulfilment of other job opportunities that match the applicant's profile, and confirms that they may be contacted about such job opportunities.