Regulatory Affairs Strategist ( Consultant ) - Clinical Development in CNS

Hourly / daily rate
06 Jan 2021
05 Feb 2021
Part Time
Contract Type
Experience Level
Senior Management

Regulatory Affairs Strategist ( Consultant ) - Clinical Development in CNS

In support of one of our UK Pharmaceutical clients, I am now recruiting for an experienced regulatory affairs specialist to support our client on an interim basis for the next few months.

Our client is in the planning stages for several new international studies, using their own drug candidate for the use in various indications with the CNS arena.   

This work will see you supporting and advising our client through the various stages of the regulatory process for 1-2 global programmes, 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 with global experience (EMEA, US/FDA etc).

This is a remote working role in the UK for an experienced, regulatory consultant.

Approx. FTE up to 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 or call +44 (0) 1239 584 300

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