Associate Scientist II, Toxicology Study Coordinator

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 - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

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.

Responsibilities:

• 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

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 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

Qualifications

Required:

• Bachelor's Degree, or equivalent education, with typically 3 or more years' experience or Master's Degree or equivalent education with 0-2 years of related experience.

• 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

Preferred Qualifications:

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

Position will be filled at level commensurate with extent of education, experience, and accomplishment. Associate Scientist I or Associate Scientist II.

Additional Information

Applicable only to applicants