Clinical Pharmacology Consultant

Entrada Therapeutics•Boston, MA
•Remote

About The Position

Entrada Therapeutics is seeking a Clinical Pharmacology Consultant to provide clinical pharmacology expertise for its clinical-stage programs. The consultant will report directly to the Head of Clinical Pharmacology and work closely with functions across the organization. The role is a U.S.-based remote contract position requiring 30–40 hours of support per week. Entrada is a clinical-stage biopharmaceutical company developing medicines intended to engage intracellular targets. Its development portfolio includes genetic medicines for neuromuscular and inherited retinal diseases, including programs for Duchenne muscular dystrophy and a partnered program for myotonic dystrophy type 1. The company describes itself as a close-knit team focused on developing therapies for patients.

Requirements

  • Master’s degree with 8 or more years of experience, Ph.D. with 3 or more years of experience, or Pharm.D. or M.D. with relevant experience, in pharmaceutical sciences, pharmacology, pharmacometrics, pharmacokinetics, or a related discipline.
  • Strong mathematical model development and analytical skills.
  • Experience using Phoenix WinNonlin, R, NONMEM, MATLAB, or other pharmacokinetic and modeling software.

Nice To Haves

  • Publication record demonstrating technical exposure to early exploratory trials through Phase 2/3 programs.
  • Compartmental PK/PD modeling experience.

Responsibilities

  • Provide clinical pharmacology input to regulatory documents.
  • Participate in clinical study design and documentation, including lab manuals, protocols, and statistical analysis plans (SAPs).
  • Independently lead and oversee the analysis, interpretation, integration, and reporting of clinical pharmacokinetic and pharmacodynamic data for assigned projects.
  • Collaborate with Clinical Development, Biostatistics, Non-Clinical Product Development, Clinical Operations, and Regulatory to support project-team and corporate objectives.
  • Monitor work performed by CROs and other external vendors to ensure compliance with agreed protocols, quality standards, and timelines.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service