**Duration: 12 months contract** **Work schedule:** + Monday - Friday / 7:30am – 4:00pm. + **1 weekend a month** on rotating shift. + 1 weekend per month on a rotating shift is preferred, however not required. Please advise if the candidate can work on weekends. **Other details:** + Tentative start date **ASAP** . + **Possible temp to perm** position. **Description:** + This position in the **In Vivo Sciences (IVS) department within the Local Delivery Safety group** is responsible for both the technical and scientific support of in vivo studies in accordance with 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. **Responsibilities:** + Provides **technical support for IVS studies** . Acts as Study Coordinator for assigned studies and demonstrates proficiency in **general in vivo procedures** . Prepares study calendar and notebook, generates data sheets, ensures study supplies are available, prepares test article formulation and handling records. + Demonstrates technical proficiency in general in vivo procedures such as **dosing, sample collection, and clinical observations of rodent and non-rodent species** . Proficient in the use of department automated data collection. + Provides assistance for short or long-term assignments in support of department functions that may include administrative or clerical duties, inventory, equipment maintenance, etc. Maintains up-to-date knowledge and skill in general dosing and sample collection procedures. **Education and Experience:** + **A.S., B.S. or B.A in a scientific** field. + High school diploma in combination with 3+ years of relevant **pre-clinical study experience** . + Experience with the conduct of **pre-clinical toxicology and/or pharmacokinetic studies** . **Essential Skills and Abilities:** + Understanding basic **pre-clinical study-related functions including dosing, observational and sampling** techniques, and study set up and management. + Strong interpersonal, organizational, problem-solving, and communication. + Demonstrated ability to work well in a team or matrix environment. + Proficiency with computer software including Microsoft Office and electronic data capture systems. + Ability to lift, stand for extended periods, perform visual examinations and manually manipulate equipment. **Top skill requirements:** + Experience working in a **research setting, animal handling** , team player, **formulation** experience. **About US Tech Solutions:** US Tech Solutions is a global staff augmentation firm providing a wide range of talent on-demand and total workforce solutions. To know more about US Tech Solutions, please visit www.ustechsolutions.com (http://www.ustechsolutionsinc.com) . US Tech Solutions is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.