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Pharmacometrician

Remote / Online - Candidates ideally in
Biddeford, York County, Maine, 04005, USA
Listing for: i-Pharm Consulting
Remote/Work from Home position
Listed on 2026-06-07
Job specializations:
  • Research/Development
    Research Scientist, Data Scientist
Salary/Wage Range or Industry Benchmark: 180000 USD Yearly USD 180000.00 YEAR
Job Description & How to Apply Below

Base pay range

$/yr - $/yr

This range is provided by i-Pharm Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more நாட்ட

Building Exceptional Biometrics & Technology Teams | Principal Consultant @ i-Pharm, Managing Consultant @ Parallel

Compensation: Up to $180,000 base 💰

Location: Fully remote anywhere in the US 🌎

Impact: Shape model‑informed drug development across a diverse portfolio spanning early research through late stage clinical programs 🎯

Benefits: Remote first culture, genuine work‑life balance, broad therapeutic exposure, program stability, and clear advancement opportunities 🌟

About

Join a leading global organization at the forefront of scientific innovation and modern drug development. With a strong record of advancing transformative therapies across multiple disease areas, this group combines deep clinical expertise with advanced quantitative approaches to accelerate decision making from early research through registration.

You will collaborate with senior experts in Clinical Pharmacology, Quantitative Sciences, and Development, contributing to a highly regarded pharmacometrics team that plays a central role in shaping program strategy. With an expanding pipeline and significant upcoming milestones, the environment offers scientific depth, long‑term stability, and impactful work.

Why This Role Matters

The organization is increasing its investment in quantitative decision making and model‑informed strategies across all development stages. As a Principal Pharmacometrician, you will define modeling approaches that influence clinical design, dose selection, regulatory strategy, and asset‑level decisions.

You will work closely with cross‑functional partners to elevate quantitative rigor across the portfolio. If you are seeking meaningful scientific impact in a collaborative, well‑resourced environment, this role offers the ownership and influence to achieve that.

What You Will Do
  • Lead development of protocols, analysis plans, PK/PD analyses, and pharmacometric reports across preclinical to Phase I through Phase IV studies
  • Advise Clinical Pharmacology teams on study design, analysis strategies, and development planning
  • Conduct a wide range of pharmacometric analyses to inform dose selection, exposure‑response, and key development decisions
  • Prepare or review PK/PD content for regulatory submissions and support agency interactions
  • Assess pharmacometric requirements for each asset and integrate modeling insights into major program milestones
  • Ensure timely, high‑quality delivery of PK/PD outcomes across assigned projects
  • Partner with colleagues across Project Management, Data Management, Biostatistics, Programming, and Medical Writing
  • Stay current on emerging techniques, literature, and regulatory perspectives within pharmacometrics and clinical pharmacology
What You Bring
  • Pharm

    D or PhD in pharmacology, pharmacometrics, pharmaceutics, biology, mathematics, engineering, statistics, or a related quantitative field
  • At least 3 years of experience in pharmacokinetics or pharmacology within industry
  • At least 2 years applying model‑based approaches in preclinical or clinical development
  • Expertise in compartmental and non‑compartmental analysis, population PK modeling, and exposure‑response approaches
  • Strong understanding of drug development, ICH GCP, and relevant regulatory frameworks
  • Strong analytical and problem‑solving skills with the ability to independently edition manage complex project components
  • Proficiency in NONMEM, R, Win Nonlin, basic SAS, and standard visualization tools
  • Strong communication skills and the ability to collaborate effectively across functions and cultures
Why It Is Special
  • Fully remote role with genuine flexibility
  • Work with highly respected scientific leaders on impactful global programs
  • Exposure to a wide variety of therapeutic areas and development stages
  • Stable, long‑term projects with continued growth potential
  • Supportive, collaborative team environment that values scientific curiosity and innovation
Seniority level

Mid‑Senior level

Employment type

Full‑time

Job function & Industries

Research, Science, and Information Technology

Biotechnology Research, Pharmaceutical Manufacturing, and Research Services

Inferred from the description for this job
  • 401(k)
  • Medical insurance
  • Vision insurance

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