Director, AI/ML for Oncology CPMS & Modeling

GSK

Waltham (MA)

On-site

USD 188,000 - 314,000

Full time

14 days+
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Benefits offered by this job

Health care benefits
Retirement benefits
Paid holidays

Job summary

GSK is seeking a Director to lead AI/ML driven modelling and simulation in Oncology Clinical Pharmacology. You will define model-based development strategies and deliver exposure–response analyses to support dose selection across programs.

You will work with cross-functional teams, applying innovative methodologies and driving regulatory submissions. A PhD in quantitative pharmacology with industry experience is required.

Qualifications

  • PhD in Quantitative Clinical Pharmacology or Pharmacometrics, or PharmD/Master with relevant experience.
  • 5+ years in mechanistic PKPD and longitudinal disease modelling with proficiency in NONMEM or R.
  • 3+ years planning and reporting clinical data analyses per industry standards.
  • Expertise applying AI/ML in Clinical Pharmacology with innovative methodologies.

Responsibilities

  • Define and execute model-based development strategies for oncology projects.
  • Plan and conduct exposure–response analyses and dose selection.
  • Apply AI/ML methods to enhance data use and trial efficiency.
  • Present and defend model-based strategies to governance boards.
  • Contribute to trial protocols, study reports and regulatory submissions.

Skills

Model-based PK/PD
AI/ML in pharmacology
Pharmacometric analysis
Regulatory submissions
Clinical pharmacology
Leadership
Cross-functional teamwork
Drug development strategy

Education

PhD in Quantitative Clinical Pharmacology
PharmD or Master with 4+ years experience

Tools

NONMEM
R

Job description

GSK is seeking a Director to lead AI/ML driven modelling and simulation in Oncology Clinical Pharmacology. You will define model-based development strategies and deliver exposure–response analyses to support dose selection across programs.

You will work with cross-functional teams, applying innovative methodologies and driving regulatory submissions. A PhD in quantitative pharmacology with industry experience is required.

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