This is an exciting opportunity for a Senior Study Director to join our clients Department of Genetic Toxicology department.
The Study Director will be responsible for setting up studies from the off-set and updating the client.
The successful candidate will:
• Be a scientific specialist and Subject Matter Expert for in vivo assays (Comet, in vivo micronucleus, transgenic mutation assays).
• Be responsible for allocated studies as described in GLP policies and take responsibility for the technical conduct of any study as well as data analysis, interpretation, documentation and reporting of results.
- Plan, design and lead a team to conduct complex studies to generate high quality scientific results
This position is suitable for a candidate possessing a PhD with relevant experience of Genetic Toxicology assays, or for a graduate or MSc level candidate with extensive experience.
Previous experience of GLP Study Directing in Genetic toxicology studies is strongly preferred. We would however welcome applications from candidates who have significant research experience in this field.
Please note that your CV should show exact dates of employment (month and year) and any gaps of a month or more should be explained.
CK Group is an Equal Opportunities employer who welcomes applications from all who meet our selection criteria.
If you do not hear back from us within 5 working days of your application for this role, it means that on this occasion you have not been shortlisted for the next stage of the recruitment campaign. Entitlement to work in the EEA is essential. Please quote reference SH41355 in all correspondence.