CMC Regulatory Affairs Manager – Office based – Hertfordshire
As we continue to provide support to one of our rare disease Pharma clients, we are now recruiting for a Regulatory Manager to work in our clients CMC division.
This position will see you working with an innovative gene therapy company with a large portfolio of clinical development programmes to treat a range of rare diseases.
Working on a range of CMC projects, you will work alongside various project teams to plan and develop regulatory strategy and preparation of various CMC documents and taking the oversight and authoring of these plans and timelines.
Working in a team environment, you will also contribute to the planning and managing of the input from the team towards the delivery and completion of these projects.
You will be managing the submissions and approval activities with a cross-functional team, help towards the planning for meetings with relevant authorities and use your CMC regulatory experience internal working practices on an ongoing basis.
If you have approx. 6-7 years’ experience of working in Regulatory Affairs, CMC (from clinical development stage) from the Biotech or Pharma industry and are interested to discuss your next career move, then get in touch me – Simon Penrose - via the contact details aside, to discuss this opportunity in more detail.
With unrivalled industry knowledge and excellent links with hiring managers in Biotechs, Pharmas and CROs throughout the UK, Europe and across the world, we would be delighted to speak with you about the role you are looking for
The number of jobs in each salary range for all:
Quay Recruitment Group Ltd
£25000/annum pension scheme, free parking
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