Senior Scientist, Clinical Pharmacology & PK/PD Modeling

Triveni Bio, Inc.

Watertown (MA)

On-site

USD 120,000 - 180,000

Full time

12 days ago

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Job summary

Triveni Bio is seeking a Senior Scientist to join the Clinical Pharmacology team. You will perform data analysis, modeling, and operational tracking across clinical-stage programs, supporting PK/PD analyses, bioanalytical strategies, and study-level pharmacology deliverables.

The role offers growth in hands-on quantitative pharmacology within a biotech setting. The ideal candidate has 2–3+ years of hands-on experience in quantitative pharmacology, with PhD or MS in a related field, and is

Qualifications

  • Ph.D. or MS in Clinical Pharmacology, Pharmaceutical Sciences, Pharmacometrics, PK/PD or related field.
  • 2+ years (Ph.D.) or 5+ years (MS) in biotech/pharma/CRO environments; postdoc may be considered.
  • Proficiency with R for data manipulation and visualization; experience with Monolix or NONMEM.

Responsibilities

  • Support development and implementation of clinical pharmacology plans for programs.
  • Design PK/PD, biomarker, immunogenicity, and exposure–response assessments in studies.
  • Perform non-compartmental analysis (NCA) using Monolix or R.
  • Do population PK/PD analyses and exposure–response modeling (R, Monolix).
  • Create graphical visualizations and tables for study updates.
  • Participate in cross-functional study teams and communicate results.

Skills

R statistics
Monolix/NONMEM
Clinical pharmacology
Regulatory documentation
Cross-functional collaboration
Travel readiness

Education

PhD or MS in Clinical Pharmacology

Tools

R
Monolix
NONMEM

Job description

Triveni Bio is seeking a Senior Scientist to join the Clinical Pharmacology team. You will perform data analysis, modeling, and operational tracking across clinical-stage programs, supporting PK/PD analyses, bioanalytical strategies, and study-level pharmacology deliverables.

The role offers growth in hands-on quantitative pharmacology within a biotech setting. The ideal candidate has 2–3+ years of hands-on experience in quantitative pharmacology, with PhD or MS in a related field, and is

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