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An opportunity for a Toxicology Study Director or Scientist to move to a desk based Regulatory Toxicology role. You will use your expert knowledge of GLP study protocols to place and monitor studies with partner CROs – you will gain full training in the safety and risk assessment aspects of the role. You will join an in-house team of toxicology and ecotoxicology specialists providing expert support to internal departments. They place a lot of studies to generate new data and would like to recruit a study protocol expert who can help in the placement and monitoring of studies. The vast majority of placed studies are in-vitro or in-silico – specific experience of a range of NAMs, in-vitro and in-silico method would be highly attractive. The team believes in development and innovation – you will receive full training in the safety and risk assessment aspects – and be encouraged to keep up to date with new emerging non-animal methods.
Job Responsibility:
Use expert knowledge of GLP study protocols to place and monitor studies with partner CROs
Gain full training in safety and risk assessment
Join an in-house team of toxicology and ecotoxicology specialists providing expert support to internal departments
Help in the placement and monitoring of studies
Keep up to date with new emerging non-animal methods
Requirements:
Proven track record in managing GLP toxicology studies
Experience with a range of in-vitro protocols
Interest in furthering expertise in in-vitro/in-silico area
Experience with a range of NAMs, in-vitro and in-silico methods (highly attractive)
Nice to have:
Experience with a range of NAMs, in-vitro and in-silico methods
What we offer:
Regulatory training
Full training in safety and risk assessment
Encouraged to keep up to date with new emerging non-animal methods