Principal Scientist II - Pharmacology

Novartis Group Companies

Cambridge (MA)

On-site

USD 126,000 - 234,000

Full time

14 days+
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Benefits offered by this job

Performance-based cash incentive
Health, life, and disability benefits
401(k) with company match
Generous time off package

Job summary

Novartis Group Companies in Cambridge, MA is seeking an in vivo scientist for their Oncology Pharmacology team. This labhead-based position involves leading studies on novel cancer therapies, particularly using in vivo models.

The ideal candidate should have a PhD and 5-8 years of relevant industry experience, especially with antibody drug conjugates and various xenograft models. The role offers a competitive salary and comprehensive benefits package.

Qualifications

  • PhD with 5-8 years of research experience in the pharmaceutical/biotech industry.
  • Deep knowledge of antibody drug conjugates is preferred.
  • Extensive experience with CDX and PDX models.

Responsibilities

  • Design pre-clinical in vivo studies to explore novel hypotheses.
  • Manage associate-level scientists.
  • Collaborate with cross-functional project teams.

Skills

Analytical Skill
Chemical Biology
Communication Skills
Molecular Biology
Drug Development
Drug Discovery

Education

PhD in a relevant field

Tools

PCR
ELISA
Western Blot
Flow Cytometry
PowerPoint

Job description

Job Description Summary

#LI-Onsite

Location: Cambridge, MA

This position is located in Cambridge, MA and does not have the ability to be located remotely. Please only apply if this area is accessible to you.

Over 40 therapies in the clinic! NIBR Oncology strives to reimagine medicines for cancer patients through a combination of treatment approaches including targeted therapies, immunotherapies, CAR‑T, and radioligand therapy. NIBR is seeking an in vivo scientist to join our Oncology Pharmacology team in Cambridge, MA. The successful candidate will join a dynamic, multi‑disciplinary team and play a key role in the development and application of in vivo models for evaluating novel cancer therapies and advancing the early‑stage drug discovery pipeline.

This is a labhead‑based position, where the ideal candidate is expected to lead efforts in the design and execution of in vivo anti‑tumor efficacy and PK/PD studies aimed at evaluating drug candidates in CDX, PDX, and syngeneic models. Applicants are expected to develop novel in vivo assays to interrogate key scientific questions and deliver high‑value translationally relevant data that can inform clinical development. Qualified candidates will have extensive experience in a variety of molecular biology skills. A strong background and expertise in antibody drug conjugates is preferred. We are looking for highly motivated, inquisitive, and creative individuals, who thrive in a highly matrixed work environment, and can effectively communicate within multidisciplinary project teams.

Job Description
Responsibilities
  • Design pre‑clinical in vivo studies to explore novel hypotheses, screen candidate molecules, and establish proof‑of‑concept of new modalities
  • Develop in vivo CDX, PDX, and syngeneic models to evaluate anti‑tumor activity, PK/PD relationships, relevant biomarkers, and key translational questions
  • Manage associate‑level scientists
  • Collaborate with cross‑functional project teams
  • Critically analyze and present results within a multidisciplinary team environment
  • Careful adherence to animal protocols and proper documentation of data and methods in electronic laboratory notebook
Qualifications
  • PhD with 5‑8 years of research experience as a postdoc or in the pharmaceutical/biotech industry
  • Deep knowledge of antibody drug conjugates
  • Extensive experience working with CDX and PDX xenograft tumor models and/or syngeneic models
  • Expertise in cell culture, PCR, ELISA, western blot, and flow cytometry
  • Strong analytical, communication (written and verbal), and organizational skills, including a proficiency with PowerPoint and commonly used data analysis programs, such as Prism and Excel
Novartis Compensation and Benefit Summary

The salary for this position is expected to range between $126,000 and $234,000 per year.

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. Employees are also 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.

Skills Desired

Analytical Skill, Analytical Skill, Analytical Thinking, Chemical Biology, Chemistry, Clinical Trials, Collaboration, Communication Skills, Curious Mindset, Data, Data Analysis, Design Of Experiments, Detail‑Oriented, Drug Development, Drug Discovery, Ethics, Gene Therapy, Immunology, Inventory Management, Laboratory, Lifesciences, Machine Learning (ML), Management, Medical Research, Molecular Biology {+ 10 more}

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