Regulatory Affairs Consultant - (Clinical Development Strategy – Neurology)

Regulatory Affairs Consultant  - (Clinical Development Strategy – Neurology)

In support of one of our oncology focused Pharmaceutical clients, I am now recruiting for an experienced regulatory affairs specialist to support our client on an interim basis.

With strong financial backing, our client is in the planning stages for several new global studies using their own drug candidate and using their unique discovery platform technology.    They are working in various oncology related fields and this project will see you working on a key molecule development to support patients with nerve damage and pain caused by chemotherapy.

This work will see you supporting and advising our client through the various stages of the regulatory process for a global programme, from Phase I- III and giving strategic input where required.

Therefore, prior experience of leading regulatory planning throughout the full life cycle of drug development will be required.   Global experience (EMEA, US/FDA etc) is required and ideally, experience in a similar field  (pain / neurology) will be highly desired.

Approx. FTE required, 0.5.

This is a great opportunity to support a new venture that is aiming to help patients with severe diseases.

To discuss this in more detail, get  in touch with me – email Simon.Penrose@rbwconsulting.com or call +44 (0) 1239 584 300