Study Director in General in Vivo Toxicology
Descrizione dell'offerta
ERBC is looking for a Study Director for General Toxicology Studies in rodents and non-rodents species in Pomezia.
The Study Director has overall responsibility for the conduct of a study as well as for the interpretation, analysis, documentation, and reporting of results.
The position requires supporting scientifically clients and other scientific / technical staff in the conduct of GLP and non-GLP toxicology studies, including study design development, managing the execution of study conduct, collecting, analyzing and interpreting data, utilization of technology and study report writing.
- Qualification
- At least two years of related experience in Pharmaceutical, Chemical or nonclinical Contract Research Organizations.
- Strong working knowledge of AAALAC and GLP regulations and preclinical testing facility operations and procedures.
- Experience of client management and technical expertise in the relevant business line.
- Education
- PhD or Master Degree in Biological Sciences, Pharm D., DVM or related discipline.
- Skills
- Excellent technical writing and computer software skills.
- Must be able to clearly speak, write, read, and understand English.
- Leadership skills for managing multidisciplinary teams for the conduct of studies or projects.
- Location
- Reference : POM001TOX
- For questions in relation to this job opportunity, please feel free to contact
- Chief Human Resources Officer, ERBC Group