AbbVie

Associate Scientist II / Scientist I, Toxicology Study Coordinator

Employer
AbbVie
Location
Lake County, IL, United States
Posted
Nov 22, 2020
Ref
2007779
Required Education
Bachelors Degree
Position Type
Full time
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines 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, eye care, virology, women's health and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on Twitter , Facebook , Instagram , YouTube and LinkedIn .

PRIMARY FUNCTION / GOALS / OBJECTIVES:
This position sits within the Preclinical Safety group at AbbVie and reports to a senior manager in Toxicology. The Associate Scientist II / Scientist I, Toxicology Study Coordinator aides in the planning, conduct and reporting of non-GLP and GLP toxicology studies, acting to support the Study Director and regulatory infrastructure.

MAJOR RESPONSIBILITIES:
  • Draft study plans, amendments, and report components
  • Assist in the technical conduct of nonclinical studies including account 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

ACCOUNTABILITY / SCOPE:
  • 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 sessions, 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

Qualifications

Basic Qualifications:
  • BS or MS in a scientific discipline and typically 2-5 (BS) or 0-2 (MS) years of relevant experience
  • Computer skills appropriate for job task
  • 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.

*Job level will be commensurate with experience

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

Significant Work Activities
N/A
Travel
No
Job Type
Experienced
Schedule
Full-time
Job Level Code
IC
Equal Employment Opportunity
At AbbVie, we value bringing together individuals from diverse backgrounds to develop new and innovative solutions for patients. As an equal opportunity employer we do not discriminate on the basis of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information gender identity or expression, sexual orientation, marital status, protected veteran status, or any other legally protected characteristic.