Regulatory Affairs Senior Manager
Regulatory Affairs Senior Manager **Urgent Requirement**Cambridgeshire or Uxbridge Contract: 6 months Hourly rate: up to £70 P/H DOERegulatory Professionals is currently collaborating with one of the world’s leading biotechnology companies. Working on innovative science and medicine. They are looking for a Regulatory Affairs Senior Manager to join their Cambridgeshire or Uxbridge team working within their oncology portfolio. The ideal candidate will have good availability to start and have previously worked as a project lead for CTA projects.Job responsibilities include and not limited to:- Leading regulatory clinical development on all EU regulatory work for assigned projects- Develop and implement regulatory strategy and executional plans - Manage regulatory submissions (CTA & MAA) for assigned products in accordance with global filing plans. - Lead the development of regional regulatory documents and meetings, and provide regulatory advice on regional regulatory requirements, mechanisms to optimize product development and to maintain compliance - Design and execute clinical development.Candidate responsibilities include:- Experience with national regulations and legislation relating to medicinal products - Strong understanding of clinical development - Strong experience in regional regulatory environment in relevant product area and development stage - Previously worked as a project leadIf you are interested in discussing this role further then please email your CV to email@example.com or call Sophie on 01189 522 979 to arrange a confidential discussion.If you are not currently looking but know someone who would be good for this role then get in touch. We offer a referral scheme at Regulatory Professionals where in which a successful recommendation will earn you £250 worth of vouchers*terms and conditions apply.