Under limited supervision, this position in the Local Delivery Safety Translational Sciences (LDSTS) department is responsible for the technical support of in vivo studies in accordance with study protocols, Good Laboratory Practice (GLP) regulations, Standard Operating Procedures (SOPs), IACUC and departmental guidelines. The position requires basic understanding of pre-clinical toxicology and pharmacokinetic study conduct in addition to knowledge of regulatory and animal welfare requirements. In collaboration with the Study Director and other relevant personnel, the incumbent will manage all technical aspects of study conduct and will generate high quality data for assigned studies.
The incumbent will also support implementation of process improvements with respect to study execution and departmental capabilities and when qualified will be responsible for training technical staff on new in vivo procedures.
Responsibilities
Discover exciting opportunities in biotech and life sciences. Join innovative companies that are advancing healthcare through cutting-edge research and technology.
Interested in building your career at AbbVie? Get future opportunities sent straight to your email.
Create AlertDiscover similar positions that might interest you
AbbVie
AbbVie
AbbVie
AbbVie
AbbVie
AbbVie