Senior ADME Scientist — Automation & AI-Driven Discovery

Novartis Group Companies

Cambridge (MA)

On-site

USD 90,000 - 183,000

Full time

9 days ago

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Benefits offered by this job

Health benefits
401(k) with company match
Generous time off

Job summary

Novartis Group of Companies in Cambridge, MA is seeking a Senior Scientist I/II to support discovery and development through in-vitro ADME assays and next‑gen lab automation for high-quality study data.

You will design, execute and report ADME experiments, interpret data for early discovery, and advance automated workflows integrated with AI-enabled analytics. Strong emphasis on cross-functional teamwork and regulatory documentation.

Qualifications

  • BSc or MSc with ADME/DMPK experience.
  • Experience in drug discovery or development lab or CRO/pharma/biotech desirable.
  • Fluent oral and written English.

Responsibilities

  • Plan, execute and report ADME assays (metabolic stability, permeability).
  • Interpret in vitro ADME data to support early discovery and optimization.
  • Advance automation strategies to expand lab capacity and standardize execution.
  • Contribute to automated, end-to-end ADME workflows with AI-enabled analytics.
  • Develop methods for bio-analysis using LCMS-MS, HRMS, ICP-MS.
  • Manage timelines and budgets; communicate data and results to teams.
  • Prepare internal ADME study reports and regulatory documents.

Skills

ADME knowledge
Lab automation
AI-enabled analytics
Metabolic stability
Permeability assays

Education

BSc in related field
MSc in related field

Tools

LCMS-MS
HRMS
ICP-MS
Automated liquid handling

Job description

Novartis Group of Companies in Cambridge, MA is seeking a Senior Scientist I/II to support discovery and development through in-vitro ADME assays and next‑gen lab automation for high-quality study data.

You will design, execute and report ADME experiments, interpret data for early discovery, and advance automated workflows integrated with AI-enabled analytics. Strong emphasis on cross-functional teamwork and regulatory documentation.

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