Associate Scientist II/Scientist I - Safety Pharmacology

About AbbVie 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. The company has a remarkable impact on people’s lives across key therapeutic areas including immunology, oncology, neuroscience, and the Allergan Aesthetics portfolio. Job Description The Safety Pharmacology department plays an influential role in AbbVie discovery projects by providing cardiovascular and neurobehavioral safety screening and developing fit‑for‑purpose assays. The focus is primarily cardiovascular safety, with additional expertise in central nervous and gastrointestinal systems and investigation of the mechanisms underlying observed toxicities. We are seeking a highly motivated individual to join our safety pharmacology team. The successful candidate should be able to: Design, develop, optimize, and validate in vitro cardiovascular, neurobehavioral, and gastrointestinal assays, including implementation and evaluation of New Approach Methodologies (NAMs) Demonstrate background understanding of electrophysiology principles with specific experience operating and troubleshooting MEA (Microelectrode Array) platforms and interpreting multi‑electrode recordings Execute complex study protocols with advanced proficiency in laboratory techniques, often in a collaborative, team‑based setting Contribute to scientific innovation through protocol optimization, troubleshooting complex issues, and potential publication or presentation of research findings Understand and implement scientific principles in research Proficient in basic lab techniques (compound dosing, rodent restraint, dilution calculations, etc.) Qualifications Bachelors Degree, or equivalent education, with 3 or more years of experience or Master’s Degree or equivalent education (Associate Scientist II) Bachelors Degree or equivalent education with 5 years of experience, or Master’s Degree or equivalent education with two years of experience (Scientist I) Demonstrate expertise in assay development, execution, and validation Advanced troubleshooting or protocol optimization skills Proven experience mentoring, training, or supervising junior scientists or technical staff Experience with peptides and/or oligo‑based modalities in an in vitro and/or in vivo setting would be beneficial Excellent verbal and written communication skills Ability to collaborate effectively within a cross‑functional team Track record of scientific contributions (publications, presentations) Good time management and multitasking skills Fast learner, able to generate and analyze data independently Proficient with Microsoft Office for data analysis Additional Information 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. Equal Opportunity Employer 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 applicants seeking a reasonable accommodation can learn more at For equal employment opportunity information, visit #J-18808-Ljbffr BioSpace