Senior Scientist, In Vivo & Translational Research

Novartis AG

Cambridge (MA)

On-site

USD 99,000 - 183,000

Full time

14 days+

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Benefits offered by this job

Performance-based incentive
Equity awards eligibility
Comprehensive benefits
Paid time off

Job summary

Novartis is seeking a Senior Scientist I or II to join Research Collaborations in Cambridge, MA, onsite. You will design, execute, and interpret complex in vivo studies across small molecules and biologics, including xRNA modalities, PK/PD, and translational endpoints.

You will lead scientific programs, collaborate with cross-functional project teams, and contribute to capability development, data-integrated decision making, and adherence to 3Rs and high ethical standards.

Qualifications

  • Bachelor or Master’s degree in Biomedical Sciences, Pharmacology, Physiology, Comparative Medicine, Life Sciences, or related discipline; recent PhD graduates considered.
  • 5+ years of relevant experience in laboratory animal research, in vivo pharmacology, translational research, or drug discovery.

Responsibilities

  • Define scientific questions and study objectives to support drug discovery and development.
  • Lead design, execution, analysis, and interpretation of complex in vivo research programs.
  • Evaluate study strategies, models, endpoints, and approaches for scientific rigor and translational relevance.
  • Integrate data streams and communicate findings to multidisciplinary stakeholders.

Skills

In vivo pharmacology
Target validation
PK/PD analysis
Data analysis with R/Python
Scientific leadership
Cross-functional collaboration

Education

Bachelor/Master/PhD in Biomedical Sciences

Tools

R
Python
Imaging analysis

Job description

Novartis is seeking a Senior Scientist I or II to join Research Collaborations in Cambridge, MA, onsite. You will design, execute, and interpret complex in vivo studies across small molecules and biologics, including xRNA modalities, PK/PD, and translational endpoints.

You will lead scientific programs, collaborate with cross-functional project teams, and contribute to capability development, data-integrated decision making, and adherence to 3Rs and high ethical standards.

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