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AbbVie
Act as Principal Investigator for bioanalytical projects, oversee sample analysis for non-clinical and clinical trials, develop and validate bioanalytical methods, and maintain/troubleshoot LC-MS systems in a regulated environment.
PhD in Analytical Chemistry or related field (or MS/BS with significant experience), with expertise in regulated bioanalysis, LC-MS systems, method development/validation, and GLP/regulatory guidelines.
The candidate for this Senior Scientist position will be working in the Regulated Bioanalysis group in the Quantitative, Translational, and ADME Sciences (QTAS) department. The primary responsibility will be acting as a Principal Investigator to manage projects and studies throughout the bioanalytical lifecycle, which includes but not limited to bioanalytical sample analysis, data review, and report writing for GLP non-clinical and clinical studies. The candidate must be experienced with managing bioanalytical operation workflows in a regulated environment. The individual will also be expected to work cross functionality within QTAS and with Preclinical Safety and Clinical Pharmacology.
Key responsibilities include:
Key Leadership Competencies:
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AI Est. Total Comp
$145,500
Location
North Chicago, IL, us
Work Type
On-site
Seniority
senior
Experience
3-5 years
Category
Research Scientist
Visa Sponsorship
Unknown
Quality Score
2.0