About AbbVie

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us atwww.abbvie.com. Follow @abbvie onLinkedIn,Facebook,Instagram,XandYouTube.

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

• Provides technical support for IVS studies with minimal supervision.
• Acts as Study Coordinator for assigned studies and assists Study Director with protocol setup.
• 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.
• Participates in training personnel in various experimental procedures and proper equipment operation
• Provides assistance for short or long-term assignments in support of department functions that may include administrative or clerical duties, report writing support, inventory, equipment maintenance, etc.
• Maintains up-to-date knowledge and skill in general animal dosing and sample collection procedures.
• Learns new techniques and concepts by reading journals, attending meetings and lectures and participating in available training and certification programs.

Qualifications

• High School/GED is required AND at least 5 years prior technical experience in area(s) of specialty
• Technical training completion/certification or associates degree may substitute for up to 2 years of required experience.
• Experience with the conduct of pre-clinical toxicology and/or pharmacokinetic studies is preferred
• Understanding of basic pre-clinical study-related functions including dosing, observational and sampling techniques in relevant laboratory animal species, and study set up and management.
• Ability to lift at least 40 pounds, stand for extended periods, perform visual examinations and manually manipulate equipment.
• Strong interpersonal, organizational, problem-solving, and verbal and written communication skills
• Demonstrated ability to work well in a team or matrix environment
• Proficiency with computer software including Microsoft Office and electronic data capture systems.

Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law:

• The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at thetimeofthis posting based on the job grade for this position.Individualcompensation paid within this range will depend on many factors including geographiclocation,andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.

• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick),medical/dental/visioninsurance and 401(k) to eligibleemployees.

• This job is eligible toparticipatein our short-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable.Theamountandavailabilityof anybonus,commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company'ssoleandabsolutediscretion unless and until paid andmay bemodifiedat the Companys sole and absolute discretion, consistent withapplicable law.

AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.

US & Puerto Rico only - to learn more, visithttps://www.abbvie.com/join-us/equal-employment-opportunity-employer.html

US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:

https://www.abbvie.com/join-us/reasonable-accommodations.html