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Job Description Summary

#LI-Onsite, Location: San Diego, California

Novartis is seeking a highly motivated ADME scientist for a laboratory-based role supporting the discovery and early development of antibody–oligonucleotide conjugates, including antibody-siRNA and antibody-PMO modalities. The successful candidate will bring hands-on experimental expertise in biotransformation, biological sample preparation, immunoprecipitation/affinity capture, LC-MS-based characterization, and in vitro/in vivo ADME workflows to enable data-driven candidate selection and translational decision-making.

Job Description Key responsibilities

• Develop and execute fit-for-purpose ADME and biotransformation workflows for antibody–oligonucleotide conjugates in biological matrices.
• Apply immunoprecipitation and affinity-capture methods to enrich antibody-conjugated species from plasma, tissue, and cellular samples.
• Use LC-MS/MS and high-resolution MS approaches to assess conjugate integrity, stability, biotransformation, and tissue biodistribution.
• Independently design, troubleshoot, and interpret in vitro and in vivo studies linking laboratory findings to PK/PD and candidate selection decisions.
• Provide ADME input to project strategy and translational decision-making in collaboration with discovery and development teams.
• Prepare clear study plans, technical reports, project summaries, regulatory content, and internal scientific presentations.
• Resolve assay and workflow challenges through practical solutions that improve data quality, throughput, and scientific impact.
• Ensure high standards of laboratory documentation, data integrity, safety, and compliance with Novartis procedures.

Essential requirements

• PhD, MSc, or BSc in pharmaceutical sciences, biochemistry, analytical chemistry, pharmacology, molecular biology, bioengineering, or a related discipline, with relevant industry experience in ADME, DMPK, biotransformation, or biologics/new modality research.
• Demonstrated hands-on laboratory experience with immunoprecipitation, affinity capture, biological sample preparation, and LC-MS/MS or HRMS-based workflows is required.
• Strong understanding of ADME principles and their application to new modalities, including oligonucleotides, antibody conjugates, biologics, or other complex therapeutics.
• Experience developing or executing LC-MS/MS or HRMS-based methods to characterize metabolic stability, biotransformation, and molecular fate of antibody–oligonucleotide conjugates.
• Ability to work effectively in a cross-functional, matrixed project environment and communicate complex scientific data clearly to project teams.
• Strong organizational skills, attention to detail, scientific rigor, and ability to manage multiple studies and priorities.
• Fluent oral and written English.

Preferred experience

• Experience with antibody–oligonucleotide conjugates, antibody-siRNA conjugates, antibody-drug conjugates, therapeutic proteins, or other targeted delivery platforms.
• Knowledge of oligonucleotide metabolism, nuclease-mediated degradation, linker stability, conjugate heterogeneity, and tissue distribution challenges.
• Experience with biological sample preparation from plasma, tissue homogenates, cells, or subcellular fractions.
• Familiarity with ligand-binding assays, hybridization-based assays, ligand capture LC-MS workflows, proteomics, or intact/protein-level mass spectrometry.
• Experience with laboratory automation, liquid handling, assay miniaturization, or higher-throughput sample preparation.
• Experience contributing to IND/IMPD-enabling packages, regulatory documentation, or project transition reports.

This is a dual posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered.

The salary for this position is expected to range between:

Principal Scientist I: $108,500 and $201,500 per year.

Principal Scientist II: $119,700 and $222,300 per year.

The final salary offered is determined based on factors like, but not limited to, relevant skills and experience, and upon joining Novartis will be reviewed periodically. Novartis may change the published salary range based on company and market factors.

Your compensation will include a performance-based cash incentive and, depending on the level of the role, eligibility to be considered for annual equity awards.

US-based eligible employees will receive a comprehensive benefits package that includes health, life and disability benefits, a 401(k) with company contribution and match, and a variety of other benefits. In addition, employees are eligible for a generous time off package including vacation, personal days, holidays and other leaves.

EEO Statement:

The Novartis Group of Companies are Equal Opportunity Employers. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, sex, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status.

Accessibility and reasonable accommodations

The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or to perform the essential functions of a position, please send an e-mail to us.reasonableaccommodations@novartis.com or call +1(877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message.

Salary Range

$108,500.00 - $201,500.00

Skills Desired

• Chemistry
• Clinical Pharmacology
• Clinical Research
• Medical Research
• Patient Care
• Physiology
• Simulation Software
• Translational Medicine