Toxicology Study Director – move into Regulatory Toxicology
Location
UK home base, Home Based
Salary
Competitive salary + regulatory training
Description
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.
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.
Key Skills
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.
Posted
Ref
VRSREG2076