Expiry Date: 26-12-2020
Category Regulatory Affairs
Salary: On Application
Job Type: Full Time
Windsor and Maidenhead
Regulatory / Regulatory Affairs Senior Manager CMC, EU & Global Development
This is a role for those who enjoy early development projects and have good experience in IND/IMPD’s for biotech or small molecule products..!
Location: M4 Corridor, Berkshire
We have a rare, unique and interesting role for one of the world’s most successful, dynamic and innovative biotechnology companies. You will be working on early stage programmes (PI & PII) for a variety of different indications including biologics, small molecules and gene therapy projects across 2 major therapy areas.
This role is responsible for providing regulatory CMC expertise into the development and implementation of the regulatory strategies, operations and planning for the CMC aspects of assigned early development programs as the regional or global Regulatory CMC Clinical lead.
What’s great about this role is not only the variety of indications that you can work on (biologics, small molecules and gene therapy projects), but you will have the scope and option to take an indication forward through the development lifecycle to MAA/BLA as well as gain vital US project exposure, which will always enhance your career further down the line.
The position is graded senior manager grade and comes with an industry high basic salary, yearly bonus and a comprehensive health and benefits plan including a high company pension contribution.
Duties and Responsibilities:
Broad background of registration experience gained from working in the pharmaceutical industry or a regulatory authority in one of the ICH regions on development and post-approval products.
To apply for this role, please press the red “Apply for position” button, or contact Theo Moore or Oli Dimitrov on +44 (0)207 801 3384 or +44 (0)207 801 3388 in full confidence to receive more details on this role or to hear about other available opportunities in Regulatory Affairs.
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