Director/Associate Director, Pharmacometrics

NS Pharma; Paramus (NJ); Hybrid; USD 190,000 - 215,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

Life Insurance

Disability Insurance

401k with match

Paid Time Off & Holidays

Career Development

Flexible Work Arrangements

Year-End Shutdown

Job summary

NS Pharma seeks a Director/Associate Director of Pharmacometrics to lead quantitative drug development across rare diseases and oncology. You will craft and execute pharmacometrics strategies, optimize dose selection, and support regulatory submissions globally.

You will mentor teams, oversee external partners, and advance pharmacometrics infrastructure and best practices, ensuring rigorous analysis and timely delivery in a matrix organization, including collaboration with the Japan team.

Qualifications

• Deep understanding of pharmacometrics and MIDD in clinical development.
• Hands-on experience with pharmacometric analyses and reporting.
• Experience building pharmacometrics infrastructure and processes.

Responsibilities

• Develop and lead pharmacometrics strategies across programs.
• Lead analyses including PK/PD, exposure-response, PBPK.
• Provide oversight for design, interpretation, and regulatory submissions.
• Mentor scientists and manage external partners.

Skills

Pharmacometric leadership

NONMEM

R

Simcyp

PK/PD analysis

MIDD strategy

Regulatory oversight

Mentoring

Education

PhD/MS/PharmD or equivalent in quantitative science

Tools

NONMEM

R

Simcyp

Job description

Director/Associate Director, Pharmacometrics

Full Time Professional PARAMUS NJ HYBRID, Paramus, NJ, US

Salary Range: $190,000.00 To $215,000.00 Annually

NS Pharma is a highly focused, research-driven biopharmaceutical company working in rare diseases. We're exploring the potential of cutting-edge science as a subsidiary of Nippon Shinyaku Co., Ltd. In Japan.

Job Summary

Provides scientific and strategic leadership in pharmacometrics to support development programs, including rare disease and oncology. Responsible for developing and executing model-informed drug development (MIDD) strategies that enable key development decisions, optimize dosing strategies, support regulatory interactions, and contribute to successful global development and regulatory approvals.

Serves as a technical leader within the organization, providing quantitative expertise, hands-on scientific leadership, and technical mentorship across global teams, including the Japan organization. Contributes to the development of organizational pharmacometrics capabilities through implementation of best practices, advancement of quantitative methodologies, and establishment of appropriate systems, tools, and infrastructure.

Essential Duties and Responsibilities

Pharmacometrics Strategy and Scientific Leadership

• Develop and execute pharmacometrics strategies across development programs to inform key development decisions, including dose selection and optimization, and study design.
• Advance organizational pharmacometrics capabilities through implementation of best practices and innovative approaches.

Clinical Development and Regulatory Support

• Lead and/or directly contribute to pharmacometric analyses, including population pharmacokinetics, exposure-response analyses, physiologically based pharmacokinetic (PBPK) modeling, and other quantitative approaches, and apply quantitative insights to address key clinical development questions.
• Provide scientific oversight and technical guidance for the design, interpretation, communication, and application of pharmacometric analyses.
• Represent pharmacometrics on cross-functional development teams, partnering closely with Clinical Pharmacology, Clinical Research, Biostatistics, DMPK, Discovery, and Regulatory Affairs to support clinical development and regulatory strategies.
• Support regulatory submissions and health authority interactions through authoring or reviewing pharmacometric sections of regulatory documents, briefing materials, submission packages, and responses to health authority questions, ensuring alignment with current regulatory expectations and industry best practices.

Technical Leadership, Capability Development and Operational Excellence

• Provide technical leadership, mentoring, and scientific coaching to pharmacometrics scientists across global locations, including members of the Japan organization.
• Establish and strengthen organizational pharmacometrics capabilities, systems, tools, workflows, and best practices to support efficient and scientifically rigorous MIDD.
• Manage and oversee pharmacometric activities conducted by external consultants, vendors, and CRO partners, ensuring timely delivery of high-quality analyses and regulatory documentation.
• Monitor emerging scientific and regulatory developments relevant to pharmacometrics and MIDD and facilitate adoption of appropriate methodologies and practices.

Supervisory Responsibility

Provides technical leadership and mentorship across pharmacometrics activities and development programs. Supports capability development across global teams, including the Japan organization, and may oversee activities conducted by external consultants, vendors, and CRO partners.

Qualifications

• Deep understanding of clinical development, clinical pharmacology, pharmacometrics, and MIDD.
• Hands-on experience with pharmacometric software and quantitative analysis tools, including NONMEM, R, Simcyp, and other relevant platforms.
• Demonstrated hands-on experience independently conducting pharmacometric analyses from analysis planning through execution, interpretation, reporting, and regulatory application, including authoring analysis plans, reports, regulatory submission documents, and responses to health authority questions.
• Demonstrated experience establishing, maintaining, and continuously improving pharmacometrics infrastructure, systems, tools, workflows, and quality processes that support efficient and scientifically rigorous MIDD.
• Demonstrated technical leadership, scientific judgment, and ability to effectively communicate and influence stakeholders in a matrix development environment.

Education and Experience

• PhD, PharmD, MS, or equivalent advanced degree in clinical pharmacology, pharmacometrics, pharmacokinetics, pharmaceutical sciences, statistics, applied mathematics, engineering, or a related quantitative scientific discipline.
• Typically 10+ years (Associate Director) or 12+ years (Director) of relevant industry experience in pharmacometrics within the pharmaceutical or biotechnology industry.
• Demonstrated experience applying pharmacometrics to support development programs from early clinical development through regulatory approval, including population PK, PK/PD, exposure-response analyses, regulatory submissions, and health authority interactions.
• Experience managing external consultants, vendors, and CRO partnerships.
• Demonstrated ability to mentor and develop scientists in pharmacometrics and quantitative drug development.

NS Pharma employees embrace our Mission to Help People Lead Healthier Happier Lives. We pride ourselves in offering employees and their families a robust Compensation and Benefits package designed to meet their needs, on and off the job.

The annualized target salary range for this role is Associate Director $190,000 to $200,000 and Director $205,000 to $215,000 actual salaries will vary and may be above or below this range depending on several factors, including experience, education, training, location, and merit.

Other benefits include:

• Medical, Dental & Vision Insurance, Basic and Voluntary Life and AD&D Insurance, Short- and Long-Term Disability Insurance, Flexible Spending Account, Health Savings Account, and Employee Assistance Programs
• Discretionary Bonus Programs and Long-term Incentive Plan
• Retirement Savings 401k with company match
• Generous Paid Time Off, Sick Time & Paid Holidays
• Career Development, Progression and Training
• Flexible Work Arrangement Programs
• Year-End Paid Holiday Shutdown