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 to manage projects throughout the bioanalytical lifecycle, including bioanalytical sample analysis, data review, and report writing for GLP non-clinical through clinical studies. The candidate must be experienced in developing and validating LC-MS based methods 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:
Qualifications:
Key Leadership Competencies:
Pay Range: $94000 – 178500 USD
Role is exclusively performed at a site or office and onsite presence is required. Employees who are site/office-based and can occasionally perform their role virtually work both in the office and remotely*, following the policies and regulations in place at their location. US Employees must be in the office on Tuesday, Wednesday, and Thursday with flexibility to work remotely on Mondays and Fridays. Three days in the office is the minimum; some individuals or teams may require more in-office days due to meetings, business/project needs or their role.
AbbVie 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 Equal Employment Opportunity Employer
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: Reasonable Accommodations
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Tagged as: Life Sciences
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