Associate Scientist, Toxicology II

Company Description

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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at  Follow @abbvie on X, Facebook, Instagram, You Tube, Linked In, and Tik Tok.

The position of Associate Scientist, Toxicology Study Coordinator is in the Preclinical Safety group and will report to a manager in Toxicology. The Associate Toxicologist aides in the planning, conduct and reporting of non‑GLP and GLP toxicology studies, acting to support the Study Director and regulatory infrastructure.

• Draft study plans, amendments, and report components
• Assist in the technical conduct of nonclinical studies including protocol set‑up in electronic data capture system and scheduling of study events
• Perform data review periodically through study conduct and at study completion
• Facilitate communications among study personnel
• Coordinate the archival of study data and specimens
• Support GLP infrastructure through quality control responsibilities and active participation in process improvement activities

• Responsible for key tasks in the set‑up and conduct of nonclinical studies
• Support the Study Director, acting as a designee for some tasks
• Study support may include data review, preparing report data tables, drafting report sections, coordinating study data archiving, and other tasks as needed
• Compile input from subject matter experts and incorporate into study plans
• Facilitate study scheduling and resource allocation
• Assist in driving assigned deliverables to timely completion
  
  Maintain training to meet compliance standards

• Bachelor’s Degree, or equivalent education, with typically 3+ years’ experience or Master’s Degree or equivalent education
  • Degree in scientific field preferred
• Aptitude for managing multiple projects in a regulated environment
• Excellent oral and written communication skills
• Proven flexibility to deal with changing timelines, shifting work priorities, and evolving regulatory/industry requirements
• Computer skills appropriate for job task

• Expertise in Good Laboratory Practices
• Previous experience in the conduct and/or reporting of nonclinical studies

• The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range.
  
  This range may be modified in the future.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to participate in our short‑term incentive programs.
• Note:
  
  No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law.

Abb Vie 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, visit  US & Puerto Rico applicants seeking a reasonable accommodation,  to learn more: