Pharmacometrician

i-Pharm Consulting; United States; Remote; USD 120,000 - 180,000; Full time

Benefits offered by this job

401(k)

Medical insurance

Vision insurance

Job summary

A leading global consulting firm is seeking a Principal Pharmacometrician to shape model-informed drug development strategies. This fully remote role offers the chance to collaborate with senior experts and contribute to impactful global programs. Ideal candidates will have a PharmD or PhD, and a strong background in pharmacokinetics. The position is full-time and provides a balanced work-life culture with significant growth opportunities.

Qualifications

• At least 3 years of experience in pharmacokinetics or pharmacology within the industry.
• Strong understanding of drug development and regulatory frameworks.
• Ability to independently manage complex project components.

Responsibilities

• Lead development of protocols and analysis plans.
• Advise on study design and analysis strategies.
• Conduct pharmacometric analyses to inform key development decisions.
• Prepare PK/PD content for regulatory submissions.

Skills

PharmD or PhD in pharmacology or related field

Experience in pharmacokinetics

Model-based approaches in development

Analytical and problem-solving skills

Proficiency in NONMEM and R

Strong communication skills

Education

PharmD or PhD in pharmacology, pharmacometrics, etc.

Tools

NONMEM

R

WinNonlin

SAS

Job description

Base pay range

$120,000.00/yr - $180,000.00/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

• PharmD 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 independentlyedition manage complex project components
• Proficiency in NONMEM, R, WinNonlin, 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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