CK Group are recruiting for a Senior Leader in non-clinical safety to join a world leading research biotechnology company in London on a permanent basis, with flexibility of hybrid working.
The Company:
Our client helps cell and gene therapy organisations across the world translate early stage research into commercially viable and investable therapies.
The Role:
Take responsibility for all non-clinical safety and provide scientific support for both internal and external projects. You will provide expert advice on assessment of the pre-clinical safety profile of candidate programs and implementation of regulatory toxicology, efficacy and other safety studies.
Responsibilities:
- Implementation and optimisation of non clinical strategies across the businesses portfolio, from pre clinical to FIH.
- Ownership of all non clinical safety packages for all programmes in the portfolio.
- Produce regulatory documentation for submission to MHRA, EMA and FDA
- Lead cross functional departments and multi-disciplinary teams
- Providing expertise in DMPK, Bioanalysis, Biomarkers, and Pharmacology.
- Leading scientific meetings and presenting data to key stakeholders
Your Background:
- PhD qualified (biological or life sciences related)
- 8 - 10 years? plus in research and development of advanced therapy medicinal products (ATMPs) with a focus on emerging technologies into early development
- Leading projects from pre-clinical to the clinic
- Leadership of non GLP and GLP regulatory complaint studies
- Extensive knowledge of ATMPs
Apply:
It is essential that applicants hold entitlement to work in the UK. Please quote job reference 53821 in all correspondence.
You must have the right to work in the UK. Learn more
- Agency: CK Group
- Reference: 53821
Website: CK Group
- Posted: 8th June 2022
- Expires: 6th July 2022