Alcon

ADME Scientist, Antibody-Oligonucleotide Conjugates (Principal Scientist I/II)

Alcon$108K — $222K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • PhD, MSc, or BSc in a related scientific discipline with industry experience in ADME, DMPK, or biotransformation.
  • Proven laboratory experience in immunoprecipitation, affinity capture, and LC-MS/MS or HRMS techniques.
  • Strong grasp of ADME principles, particularly in relation to oligonucleotides and antibody conjugates.
  • Experience in developing LC-MS/MS or HRMS methods for analyzing antibody-oligonucleotide conjugates.
  • Ability to work efficiently in cross-functional teams and communicate complex scientific findings clearly.
  • Strong organizational skills with attention to detail and multi-study management capabilities.
  • Fluency in oral and written English.

Responsibilities

  • Develop and implement tailored ADME and biotransformation workflows for conjugate analysis.
  • Apply immunoprecipitation and affinity capture techniques for sample enrichment.
  • Use LC-MS/MS for evaluating conjugate stability and biodistribution.
  • Design and interpret in vitro and in vivo studies for candidate selection.
  • Contribute ADME insights to project strategies and decisions with teams.
  • Prepare technical reports and regulatory documentation clearly and effectively.
  • Troubleshoot assay challenges to enhance data quality and throughput.
  • Maintain high laboratory standards and compliance with safety procedures.

Benefits

  • Comprehensive health, life, and disability benefits.
  • 401(k) plan with company contribution and match.
  • Generous time-off package including vacations, personal days, and holidays.
Full Job Description
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.

To learn more about the culture, rewards and benefits we offer our people click here.

Salary Range
$108,500.00 - $201,500.00

Skills Desired
Chemistry, Clinical Pharmacology, Clinical Research, Medical Research, Patient Care, Physiology, Simulation Software, Translational Medicine

About Alcon

Alcon is a global medical company specializing in eye care products and services. The company's products include surgical equipment, contact lenses, and eye drops. Alcon was founded in 1945 and is headquartered in Baar, Switzerland. The company operates in over 70 countries and has over 20,000 employees. In 2019, Alcon became an independent publicly traded company after being spun off from Novartis.
Learn more about Alcon
Size
24,389 employees
Market Cap
$33.3 billion
Industry
Founded
1945
NASDAQ

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