1

Pharmacometrics Jobs (NOW HIRING)

About This Role Pharmacometrics analyses and insight are critical in the development of drug candidates, determination of product viability, and maximization of commercial value at Biogen. As the ...

About This Role Pharmacometrics analyses and insight are critical in the development of drug candidates, determination of product viability, and maximization of commercial value at Biogen. As the ...

$191 - $300/hr

Director, Quantitative Pharmacology and Pharmacometrics - OncologySkip to main content*This site uses cookies to provide you with an optimal user experience. The cookies include Strictly Necessary ...

New

next page

Showing results 1-20

Pharmacometrics information

See salary details

$142.5K

$242.4K

$390K

How much do pharmacometrics jobs pay per year?

As of Aug 21, 2026, the average yearly pay for pharmacometrics in the United States is $242,400.00, according to ZipRecruiter salary data. Most workers in this role earn between $179,500.00 and $286,000.00 per year, depending on experience, location, and employer.

What is pharmacometrics?

A Pharmacometrics job involves using mathematical models and statistical techniques to quantify drug effects, optimize dosing, and support decision-making in drug development. Professionals in this field analyze pharmacokinetic (PK) and pharmacodynamic (PD) data to predict drug behavior and improve therapeutic outcomes. They work closely with clinical pharmacologists, statisticians, and regulatory experts to enhance drug safety and efficacy. Typical roles exist in pharmaceutical companies, regulatory agencies, and academia, helping to streamline drug approval and development processes.

What does a pharmacometrics professional do?

As a pharmacometrician, your typical responsibilities include designing and executing pharmacokinetic and pharmacodynamic models, analyzing clinical trial data, and providing quantitative support for drug development decisions. You will collaborate closely with clinical pharmacologists, statisticians, and regulatory teams to optimize study design, dosing regimens, and data interpretation. The workflow often involves managing multiple modeling projects, attending cross-functional meetings, and preparing reports for both internal teams and regulatory submissions. This role offers the opportunity to work at the intersection of science and data to influence critical stages of pharmaceutical research and development.

What are the key skills and qualifications needed to thrive in pharmacometrics?

To thrive in pharmacometrics, you need a solid background in pharmacokinetics, pharmacodynamics, statistics, and mathematical modeling, usually supported by an advanced degree in pharmacy, pharmacology, or a related field. Proficiency with software such as NONMEM, R, Monolix, or SAS, as well as familiarity with regulatory guidelines, is highly valued. Strong analytical thinking, collaboration, and effective communication skills set top performers apart in this discipline. These abilities allow pharmacometricians to generate and interpret complex data, inform drug development decisions, and work efficiently within multidisciplinary teams.

Are pharmacometricians in demand?

Pharmacometricians are in increasing demand due to the growing emphasis on model-informed drug development and personalized medicine. They typically work in pharmaceutical companies, research institutions, and regulatory agencies, often requiring skills in pharmacokinetics, pharmacodynamics, and modeling software like NONMEM or R. The field offers strong job prospects as the industry seeks professionals with expertise in quantitative analysis and drug development processes.

How do I become a pharmacometrician?

To become a pharmacometrician, typically a candidate needs a graduate degree such as a master's or Ph.D. in pharmacometrics, pharmacology, biostatistics, or a related field. Strong skills in pharmacokinetic/pharmacodynamic modeling, programming (e.g., R, NONMEM), and understanding of clinical trial data are essential. Gaining experience through internships or collaborative research can also improve job prospects.

How much does a pharmacometrician make?

The average salary for a pharmacometrician typically ranges from $80,000 to $130,000 annually, depending on experience, education, and location. Senior professionals with advanced skills in pharmacokinetics and pharmacodynamics can earn higher salaries, especially in pharmaceutical or biotech industries.

What does a pharmacometrician do?

A pharmacometrician analyzes clinical and pharmacological data to develop models that predict drug behavior and optimize dosing. They use statistical and computational tools to support drug development, regulatory submissions, and personalized medicine. Strong skills in pharmacokinetics, pharmacodynamics, and modeling software are essential for this role.
More about Pharmacometrics jobs

What cities are hiring for Pharmacometrics jobs?

Cities with the most Pharmacometrics job openings:

What are the most commonly searched types of Pharmacometrics jobs?

The most popular types of Pharmacometrics jobs are:

What states have the most Pharmacometrics jobs?

States with the most job openings for Pharmacometrics jobs include:

Infographic showing various Pharmacometrics job openings in the United States as of August 2026, with employment types broken down into 97% Full Time, 1% Part Time, 1% Temporary, and 1% Contract. Highlights an 63% Physical, 24% Hybrid, and 13% Remote job distribution, with an average salary of $242,400 per year, or $116.5 per hour.

Senior Director, Advanced Pharmacometrics, Quantitative Pharmacology and Pharmacometrics - Immuno-On

Merck & Co.

Upper Gwynedd, PA • On-site

Full-time

Medical, Dental, Vision, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Merck rating

8.0

Company rating: 8.0 out of 10

Based on 51 frontline employees who took The Breakroom Quiz

43rd of 86 rated pharmaceutical


Job description

Job DescriptionWe are seeking an accomplished scientific leader to join the Quantitative Pharmacology and Pharmacometrics - Immuno-Oncology (QP2-IO) team as-Senior Director, Advanced Pharmacometrics. QP2-IO is part of the Global Clinical Development organization and is responsible for clinical pharmacology and pharmacometrics strategy and execution for oncology assets, from candidate nomination through registration.Our Senior Directors are recognized experts in quantitative drug development and possess a deep, integrated understanding of both the science and the strategic, end-to-end dimensions of oncology drug development. Reporting directly to Executive Director and Section Head, QP2-IO, the Senior Director will lead advanced pharmacometrics strategy and implementation to inform key oncology portfolio decisions. -The ideal candidate is an accomplished scientific leader with deep expertise in oncology drug development and has a proven track record in shaping and delivering impactful oncology MIDD strategies. This individual must have extensive experience in population PK/PD, tumor dynamics and survival modeling, Bayesian inference, and model-based meta-analysis (MBMA), along with strong cross-functional influencing skills in a matrixed environment. The role includes substantial internal and external engagement, including with vendors and regulatory agencies.Primary ResponsibilitiesStrategic LeadershipLead quantitative pharmacology strategy across the oncology portfolio, ensuring alignment with program goals and organizational priorities.Develop and implement long-range plans for integrating MIDD, pharmacometrics, data science, and Bayesian modeling approaches to accelerate and de-risk oncology drug development.Partner with senior leaders in Clinical Development, Translational Medicine, Biostatistics, Regulatory, and Data Science to define modeling strategies that influence program design and key decisions.Scientific & Technical LeadershipOversee development of advanced pharmacometrics modeling including but not limited to population PK/PD, tumor dynamics and survival modeling, advanced models to inform dose selection, clinical design, and benefit-risk assessments.Champion the use of Bayesian methods including hierarchical and joint modeling, and prior-data integration to strengthen oncology decision-making.Ensure high-quality, regulatory grade pharmacometric deliverables for submissions, label negotiations, and scientific advice meetings.Stay at the forefront of emerging methodologies including AI/ML and promote innovation in modeling tools, computational frameworks, and analytics platforms.Team Leadership & DevelopmentLead, mentor, and develop a team of quantitative scientists in a matrixed role.Foster a culture of scientific rigor, excellence, collaboration, and innovation.Cross-Functional CollaborationCollaborate with QP2 leads to design efficient, model-informed clinical trialsWork closely with Translational, Clinical, Biostatistics functions to integrate advanced modeling into decision frameworks.Regulatory & External EngagementContribute to regulatory strategy through preparation of pharmacometric reports, briefing documents, and presentations.Represent the company at scientific conferences, external collaborations, consortia, and industry working groups.Minimum EducationPh.D.-in pharmacokinetics/pharmacodynamics, pharmacometrics, mathematics, statistics/biostatistics, chemical/biomedical engineering, or a related discipline with-at least 10 years-of pharmaceutical drug development experience, including substantial experience in pharmacometrics roles. OR Master's, PharmD, or equivalent degree-with-at least 15 years-of pharmaceutical drug development experience, with a demonstrated record of increasing responsibility, independence, and leadership in similar roles.Required Experience and SkillsExtensive and in-depth experience in application of MIDD in oncology drug development to drive impactful development decisions.Deep proficiency in advanced pharmacometrics methods such as:Bayesian hierarchical models, joint models of tumor and survival, drop-out models, MBMA, advanced clinical trial simulation methods, integrating PROs and RWD into traditional NLME approaches. -Hands-on experience with software such as NONMEM, Pumas, Stan, R, and/or other Bayesian platforms.Advanced analytical skills, including designing and interpreting clinical trials, problem solving, critical data analysis, interpretation, and decision making.Understanding of oncology biology, translational pathways, and clinical endpoints (e.g., ORR, PFS, OS, tumor dynamic modeling).Demonstrated impact across multiple therapeutic modalities, including, for example, antibody-drug conjugates (ADCs), T cell engagers (TCEs) monoclonal antibodies (mAbs), cytokines, and small molecules.Experience integrating AI/ML methods into clinical pharmacology and pharmacometrics workflows to advance model-informed drug development, optimize study design, and support regulatory decision-making is preferred.Excellent written and verbal communication skills, with a track record of effective cross-functional collaboration, stakeholder management in a matrixed environment and ability to influence at senior levels.#QP2#Eligible for ERPThe remote position is only applicable for those that are not within commutable distance to primary sites noted in posting.- If commutable, the position will be hybrid. Please note that standard commute is (less than) Required Skills: Biopharmaceutical Industry, Clinical Development, Cross-Functional Collaboration, Data Modeling, Data Science, Data Visualization, Drug Development, Effective Written Communication, Model Driven Development, Modeling Software, Nonlinear Mixed Effects Modeling (NONMEM), Oncology Drug Development, Pharmacodynamics, Pharmacokinetics, Pharmacometrics, Verbal CommunicationsPreferred Skills: Artificial Intelligence (AI), Bayesian Models, Machine Learning (ML), Multiple Therapeutic Areas, PKPD Modeling, Population PharmacokineticsCurrent Employees apply HERE Current Contingent Workers apply HERE US and Puerto Rico Residents Only:Our company is committed to inclusion, ensuring that candidates can engage in a hiring process that exhibits their true capabilities. Please click here if you need an accommodation during the application or hiring process. As an Equal Employment Opportunity Employer, we provide equal opportunities to all employees and applicants for employment and prohibit discrimination on the basis of race, color, age, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability status, or other applicable legally protected characteristics.--As a federal contractor, we comply with all affirmative action requirements for protected veterans and individuals with disabilities.- For more information about personal rights under the U.S. Equal Opportunity Employment laws, visit:EEOC Know Your Rights EEOC GINA Supplement• We are proud to be a company that embraces the value of bringing together, talented, and committed people with diverse experiences, perspectives, skills and backgrounds. The fastest way to breakthrough innovation is when people with diverse ideas, broad experiences, backgrounds, and skills come together in an inclusive environment. We encourage our colleagues to respectfully challenge one another's thinking and approach problems collectively.Learn more about your rights, including under California, Colorado and other US State Acts The salary range for this role is$210,400.00 - $331,100.00This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.We offer a comprehensive package of benefits.- Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at https://jobs.merck.com/us/en/compensation-and-benefits .You can apply for this role through https://jobs.merck.com/us/en (or via the Workday Jobs Hub if you are a current employee). The application deadline for this position is stated on this posting. San Francisco Residents Only: -We will consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents Only: -We will consider for employment all qualified applicants, including those with criminal histories, in a manner consistent with the requirements of applicable state and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance Search Firm Representatives Please Read Carefully-Merck & Co., Inc., Rahway, NJ, USA, also known as Merck Sharp & Dohme LLC, Rahway, NJ, USA, does not accept unsolicited assistance from search firms for employment opportunities. All CVs / resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. -No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. Where agency agreements are in place, introductions are position specific. Please, no phone calls or emails.-Employee Status: RegularRelocation:No relocationVISA Sponsorship:Yes Travel Requirements: 10%Flexible Work Arrangements:Not ApplicableShift:Not IndicatedValid Driving License:NoHazardous Material(s):n/aJob Posting End Date:09/4/2026 *A job posting is effective until 11:59:59PM on the day BEFORE -the listed job posting end date. Please ensure you apply to a job posting no later than the day BEFORE the job posting end date. Requisition ID:R408271 Salary: . Date posted: 08/18/2026

What Merck employees say

Pay

Benefits

Hours and flexibility

Workplace

Get the full story on Breakroom