PK/PD Modeling Scientist — Dose Design & QSP

Hemab Therapeutics

Boston (MA)

On-site

USD 120,000 - 180,000

Full time

5 days ago
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Job summary

Hemab Therapeutics, a clinical-stage biotech with offices in Cambridge, MA, USA and Copenhagen, DK, seeks a Scientist for PK/PD Modeling & Simulation. You will develop population PK/PD, exposure–response, and QSP models to support dose selection and trial design, collaborating with clinical pharmacology, regulatory, biometrics, and outside partners.

You will validate models, run simulations, interpret data, and contribute to regulatory submissions while keeping modeling strategies aligned with

Qualifications

  • Ph.D. required in Pharmacometrics, Clinical Pharmacology, Pharmacokinetics, or related field.
  • Hands-on PK/PD modeling experience with population approaches.
  • Experience communicating quantitative findings to cross-functional and regulatory teams.

Responsibilities

  • Develop, validate, and apply population PK/PD, exposure–response, PBPK and QSP models.
  • Run simulations to inform dose selection and trial design.
  • Interpret PK/PD data and translate into actionable program guidance.
  • Contribute to regulatory submissions and respond to agency questions.
  • Collaborate across cross‑functional teams to integrate modeling insights.
  • Stay current with regulatory expectations and new quantitative methods.
  • Issue management for modeling deliverables with vendors/consultants.
  • Act as a proactive team player, embracing feedback and goals.

Skills

NONMEM
Monolix
Phoenix NLME
R
MATLAB
PK/PD modeling
Regulatory communication

Education

Ph.D. in Pharmacometrics
Clinical Pharmacology
Pharmacokinetics
Applied Mathematics
Statistics

Job description

Hemab Therapeutics, a clinical-stage biotech with offices in Cambridge, MA, USA and Copenhagen, DK, seeks a Scientist for PK/PD Modeling & Simulation. You will develop population PK/PD, exposure–response, and QSP models to support dose selection and trial design, collaborating with clinical pharmacology, regulatory, biometrics, and outside partners.

You will validate models, run simulations, interpret data, and contribute to regulatory submissions while keeping modeling strategies aligned with

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