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Principal Scientist Ii To Senior Principal Scientist, Clinical Pbpk Modeling & Simulation

3-6 years
USD 152,600 – 283,400
10 Nov. 26, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Principal Scientist II / Senior Principal Scientist – Clinical PBPK Modeling & Simulation

Location: Cambridge, Massachusetts, USA
Job Type: Full-Time | Onsite (No Remote Option)
Experience Required: 3–6+ years industry experience depending on level

Overview

Novartis is hiring a Principal Scientist II or Senior Principal Scientist to join the Modeling & Simulation group within PK Sciences. This dual-level role focuses on developing and applying advanced physiologically based pharmacokinetic (PBPK) models to support drug discovery, translational research, and global clinical development.

The position is based onsite in Cambridge, MA and supports strategic decision-making across multiple therapeutic areas by enabling reliable DDI assessments, biopharmaceutics evaluations, human PK predictions, and population-specific exposure modeling.

This opportunity is suited for experienced PBPK modelers with a strong background in ADME, pharmacokinetics, and regulatory interactions.

Key Responsibilities

  • Lead PBPK modeling activities to support global drug development, discovery programs, and translational research.

  • Perform predictive PBPK analyses for human PK, drug–drug interaction (DDI) potential, disease-related exposure changes, and pediatric or special-population considerations.

  • Support formulation decisions and biopharmaceutics assessments using mechanistic absorption and disposition modeling.

  • Integrate ADME, PK/PD, and DDI data into robust translational modeling strategies.

  • Interpret, document, and communicate modeling insights to cross-functional project teams.

  • Prepare high-quality summaries for regulatory submissions and independently address health authority queries.

  • Ensure modeling work aligns with regulatory guidance and global industry standards.

  • Contribute to clinical development strategies by using model-informed approaches to optimize trial design and enable clinical waivers.

Essential Qualifications

  • PhD in Pharmaceutical Sciences, Pharmacokinetics, Biopharmaceutics, ADME/DMPK, or related scientific discipline.

  • Principal Scientist II: Minimum 3 years of industry experience in PBPK modeling and simulation.

  • Senior Principal Scientist: Minimum 6 years of industry experience in PBPK modeling and simulation.

  • Hands-on proficiency with PBPK platforms such as PK-Sim, Simcyp, or GastroPlus.

  • Experience with additional modeling tools (Monolix, R, Phoenix, NONMEM) is preferred.

  • Demonstrated contribution to regulatory documents and familiarity with global health authority expectations.

  • Broad understanding of drug discovery and development, including PK, ADME, formulation, drug delivery, and DDI mechanisms.

Preferred Skills

  • Strong scientific leadership, analytical thinking, and problem-solving abilities.

  • Ability to communicate complex data clearly to multidisciplinary stakeholders.

  • Proven track record supporting model-informed drug development strategies.

  • Ability to work in dynamic, fast-paced environments and manage multiple timelines.

Compensation

Principal Scientist II: USD 119,700 – 222,300 annually
Senior Principal Scientist: USD 152,600 – 283,400 annually

Final compensation is based on experience, expertise, and internal alignment. Eligible roles may receive performance-based bonuses and annual equity awards.

Benefits

Qualified US-based employees receive:

  • Comprehensive health, life, and disability coverage

  • 401(k) with company match and contributions

  • Generous paid time off including vacation, personal days, holidays, and special leaves

  • Additional programs supporting professional and personal development

About Novartis

Novartis is committed to accelerating scientific breakthroughs that transform patient lives. The organization values innovation, integrity, performance, and cross-functional collaboration. To learn more about culture, benefits, and career development opportunities, visit the Novartis careers site.

Equal Opportunity Statement

Novartis is an Equal Opportunity Employer and does not discriminate based on race, color, religion, gender, national origin, age, sexual orientation, gender identity, disability, veteran status, or any legally protected characteristics.

Accessibility & Accommodations

Candidates requiring reasonable accommodation for the application or hiring process may contact the Novartis accommodations team at +1 (877) 395-2339 or via email, referencing the job requisition number.