Toxicology Study Director – move into Regulatory Toxicology

UK home base, Home Based

Competitive salary + regulatory training

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 CRO s – 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 NAM s, 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.

We are looking for a Study Director or Study Scientist with a proven track record in managing GLP toxicology studies – ideally you will have experience with a range of in-vitro protocols and be interested in furthering your expertise in this area. An excellent career development opportunity.

Toxicology, safety assessment, hazard assessment, regulatory toxicology, NAM , in-vitro, in-silico methods, innovation, toxicology support, presentation, regulatory science, method innovation, communication.

VRS Regulatory is the Regulatory Affairs and Risk Assessment division of specialist scientific recruiter VRS . We focus on recruitment in Regulatory Affairs, Registrations, REACH , CLP , SDS Authoring, Product Safety, Compliance, Risk Assessment, Regulatory Toxicology, Regulatory Ecotoxicology and Environmental Fate in the chemicals, agrochemicals and biocides sectors.