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Translational Scientist

Partnership Jobs
Job LocationNew Town, Edinburgh
EducationNot Mentioned
SalaryCompetitive salary
IndustryNot Mentioned
Functional AreaNot Mentioned
Job TypePermanent, full-time

Job Description

Translational ScientistLocation: Stratford, London (Were happy to talk about flexible working)Salary: £40,000- 50,000Contract: Permanent, full timeClosing date: 22nd SeptemberCould you help us plan and implement pharmacology and toxicology packages to support submissions for vaccines, cell therapies, small molecules or biologicals Why we need youCancer Research UKs Centre for Drug Development (CDD) is a centre of excellence in early phase cancer drug development. We provide the expertise, facilities and close connections with industry and academia to translate todays science into tomorrows medicine. We have a pioneering portfolio with a focus on developing First-in-Class therapeutic agents. We currently have over 20 projects in active development including antibodies, cell therapies, vaccines and small molecules.The CDD Translational Sciences team is an established and experienced group of clinicians, biomarker scientists and translational scientists. The successful candidate will independently represent the translational group on a number of multidisciplinary project teams delivering our portfolio of projects. We are looking for a scientist with solid experience of delivering components of toxicology and pharmacology packages to support First-in-Human studies, and the ability to interpret internal and published data to make recommendations to project teams.What skills are we looking forYoull be able to bring to the role:

  • Experience of planning, executing and interpreting pharmacology and/or toxicology studies, including working with contract research organisations
  • The ability to carry out thorough reviews of the science and regulatory requirements around your projects and recommend appropriate preclinical packages
  • Technical experience in one of more of the following: Regulated bioanalysis, PK analysis or modelling, Toxicology, Bioinformatics, Oncology models
  • Ability to apply yourself to multiple projects spanning a range of therapeutic modalities
    • What will I be doing Make an impact every day by:
  • Designing and delivering and documenting preclinical studies and/or scientific justifications adequate to support acceptance of clinical trial authorisation applications.
  • Authoring non clinical components of protocols and other regulatory documents to support First-in-human studies
  • Working closely with project teams, clinical investigators and scientific experts to inform the design of First-in-Human clinical trials
  • Supporting the interpretation of emerging data from clinical trials.
    • What will I gainWithout you we wouldnt be able to achieve our aim of seeing 3 in 4 people survive cancer by 2034. So we want to reward you in as many ways as possible. Our benefits package includes discounts on anything from travel to technology, generous holiday allowance, gym membership, childcare vouchers and much more. Youll also be able to access a wide range of learning and development opportunities. And ultimately youll know that youll be changing lives through your work. If youre as ambitious as we are, join our collective force and enjoy an excellent career, as we save lives and add years.

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