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Principal Scientist, Pharmacometrics

Posted 10 days agoViewed

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💎 Seniority level: Principal, 4+ years

📍 Location: United States

🔍 Industry: Biopharmaceutical

🏢 Company: Entrada Therapeutics👥 101-250💰 $100,000,000 Post-IPO Equity 8 months agoBiotechnologyEmergency MedicineMedicalHealth CareGenetics

🗣️ Languages: English

⏳ Experience: 4+ years

🪄 Skills: Project ManagementData AnalysisDifferential EquationsMatlabAlgorithmsCommunication SkillsAnalytical SkillsMicrosoft OfficeDocumentation

Requirements:
  • Ph.D. in pharmaceutical sciences, pharmacology, pharmacometrics, pharmacokinetics, or related discipline or Pharm.D. or M.D. with relevant experience.
  • 4+ years’ experience with background in the application of mathematical, pharmacokinetics, and statistical methods within pharma/biotech industries or drug development.
  • Experience using Phoenix WinNonlin, R, NONMEM, MATLAB, or other pharmacokinetic and modeling software.
  • Strong mathematical model development and analytical skills.
  • Proficient documentation and organizational skills, as well as proven ability to be self-motivated and able to work independently.
  • Excellent communication and presentation skills to efficiently relay information to project teams and other key stakeholders.
  • Ability to travel approximately 15% of the time, as determined by the needs of the business.
Responsibilities:
  • Use modeling approaches to advance clinical and translational research at Entrada Therapeutics.
  • Lead cross-functional teams with scientific acumen to develop and execute. pharmacometrics for programs across all phases of drug development.
  • Support the development of diverse modeling strategies and execution, in collaboration with the Head of Clinical Pharmacology, to bring value to the Entrada portfolio.
  • Work collaboratively with functional partners, including Clinical Development, Biostatistics, Non-Clinical Product Development, Clinical Operations, and Regulatory to deliver on both project team and corporate objectives.
  • Author regulatory documents including analysis plans, study reports, population PK reports, exposure-response analyses reports and other similar documents.
  • Monitor work with CROs and other external vendors to ensure compliance with agreed protocols, quality standards, and timelines.
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