Principal Research Scientist Job North Chicago area,Illinois USA,Science

Position: Principal Research Scientist I

About Abb Vie

Abb Vie'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 Abb Vie, please visit us Follow @abbvie onLinked

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Company Description About Abb Vie

Job Description Purpose

We areseekingahighly-motivated toxicologist to support discovery-stage programs across therapeutic areas within preclinical safety. As part of the Investigative Toxicology and Pathology group,the successful candidate will effectivelyleveragein silico, in vitro, and in vivo tools to design and execute a safety assessment strategy to support pipeline advancement.

Asprojecttoxicologist, this scientist will work cross-functionally, providing critical subject matterexpertiseand data integration to drive progress for programs.

Responsibilities

Support project teamsto design and execute a safety strategy specific to the needs of the projectbyleveraginginternal and external resources, in silico tools, in vitro models, and in vivo studies. Select and design experiments that answer key questions, are decision-enabling, and promote judicious progression of programs.
Support development and deployment ofin vitro tools for safety assessment (simple and complex in vitro models, or NAMs) andutilizeappropriate endpoints(imaging,toxicogenomic,etc) to support decision-making.
Demonstrate the ability toidentifyandresolve key project hurdles by effectivelyutilizingavailable information and resources.
Communicate effectively across cross-functional teams andwithleadership to support alignment on program strategy.
Proactively seek outnew information in the literature and incorporate this into individual projects as well as the overall safety assessment strategy.
Seize opportunities to pursue project-relevant exploration and experiments to support data-driven decision-making and program progress.
May mentor/supervise a team of one ormoreand evaluate the performance of those individuals;accountable for the effective performance of the team/individuals.
Collaborate effectively with other teams toidentifyareas of scientific advancement and efficiency.

Qualifications Required

Bachelors Degree or equivalent education and extensive,typically 14+years of experience,Masters Degreeor equivalent education and typically 12years of experience, PhD and typically6+years of experience.
Experience directing the use of,and interpreting data from,in vitro safety studies.
Demonstrateabilityto function independently, generating original research or development strategies.
Possess thorough theoretical and practical understanding ofownscientific discipline.
Effective writer and communicator of research.

Demonstrated scientific communication and presentation skills.

Preferred

People leadership and management experience
DABT board certification or equivalent
Experience working on cross-functional project teams, including but not limited to, within pharmaceutical development

Additional Information

The compensation range described below is the range of possible base pay compensation that the Company believes ingood faith it will pay for this role at the timeof this posting based on the job grade for this position.

Individual compensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.
We offer a comprehensive package of…