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Biological Efficacy Manager - Lead

Application Deadline: 31st August 2020

Manager – Biological Efficacy (Lead)                                            c94-118k + Strong Bonus                

South East                                                                                           Ref: ABJ4801

 

As Lead Biological Efficacy Manager within the Biological Efficacy Assessment team you will shape and direct biological efficacy assessment strategies to deliver transformational skills and capabilities to validate the efficacy of candidate active compounds and products for a global company. As Biological Efficacy Manager managing a small team you will direct the work of the team in the areas of disease modelling, cell biology, toxicology and bioinformatics / computational biology.

 

With a strong background in biological sciences, pharmacology or toxicology you will lead the biological science efficacy assessment of products in order to build internal scientific knowledge, support regulatory engagement and compliance and consumer claims across new product categories.   Your strategic research will provide a weight of evidence approach to support internal company positions, external claims and scientific publications.

 

Key Responsibilities

 

  • Shape and direct biological efficacy assessment strategies to deliver transformational skills and capabilities to validate the efficacy of candidate compounds and products



  • Direct the work of the team in the areas of disease modelling, cell biology, next generation toxicology and bioinformatics / computational biology.

  • Highly qualified in the area of disease modelling, adverse outcome pathways and toxicology you will be able to set the strategy for the team in terms of new assays for mechanistic understanding and develop effective approaches for biological data integration in order to deliver scientific insights to support successful product launches and to monitor the competitor landscape.



  • Lead/participate in relevant cross-R&D and cross-functional activities to drive new active science agenda.

  • Interface with all new product / discovery teams to build in relevant workstreams to expand knowledge.

  • Manage external collaborations with thought leaders, institutes, start-ups and multinationals.

  • Develop peer-reviewed scientific papers and present at relevant external forums.


 

Qualifications, Education and Experience:-

  • Qualified to PhD level in biological sciences, pharmacology or toxicology

  • Lead and shape future developments across in-vitro biology, dosimetry and toxicology.

  • Experience with in-vitro / in-silico methods of working to study human effects

  • Lead and shape future developments across in-vitro biology, dosimetry and toxicology.

  • Working with 3rd parties to ensure they meet requirements for biological efficacy assessment

  • Lead and contribute to regulatory dossier preparations, external communications and publications.

  • Professional experiences in delivering regulatory packages to support potential claims.

  • Strong leadership, collaboration and communication skills, within a community of SMEs.



  • Inspire, motivate and lead your team and support the wider R&D community and stakeholders in line with the company’s overall business demands and priorities.



  • Ability to attend F2F meetings and to travel domestically and internationally as and when required.


 

They can offer an attractive salary, commensurate with qualifications and experience as well as a Strong Bonus Scheme (90%), Car Allowance (c6k), Share Options, Contributory Company Pension Scheme and Subsidised Private Medical Insurance as part of a strong flexible benefits package.

 

To Apply Please contact Alison Basson at, quoting reference - Ref: ABJ4879  on 0203 909 3782, 07814547440 or reply via email, entering the job title and reference code in the subject field to alison.basson@hudsonshribman.co.uk

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