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Contract Dmpk Jobs (NOW HIRING)

Calibr

SENIOR DIRECTOR, TOXICOLOGY

San Diego, CA · On-site

Partner cross-functionally with Chemistry, Biology, DMPK, CMC, Regulatory, and Clinical teams to ... Oversee and manage multiple contract research organizations (CROs) supporting outsourced toxicology ...

Calibr

SENIOR DIRECTOR, TOXICOLOGY

San Diego, CA · On-site

Partner cross-functionally with Chemistry, Biology, DMPK, CMC, Regulatory, and Clinical teams to ... Oversee and manage multiple contract research organizations (CROs) supporting outsourced toxicology ...

Iambic Therapeutics, Inc

$164K - $245K/yr

This role partners closely with Clinical Development, DMPK, Biostatistics, and Regulatory Affairs ... industry, contract research, or clinical research. * Experience with clinical development of ...

New

Frontage-Laboratories

Principal Scientist

Exton, PA · On-site

$120 - $160/hr

DMPK (Drug Metabolism & Pharmacokinetics) Employment Type: Full-Time Company Frontage Laboratories Inc. is an award winning, publicly listed, full-service CRO/Contract Research Organization operating ...

Frontage Laboratories

Scientist

Hayward, CA · On-site

$80K - $110K/yr

... Contract Research Organization operating over 25 state-of-the-art laboratories across the US ... DMPK (Drug Metabolism and Pharmacokinetics) and its impact on drug safety and efficacy. Roles ...

Clinical Dynamix, Inc.

Project Manager R&D

Jersey City, NJ · Hybrid

$125K - $150K/yr

... DMPK/ADME, and bioanalysis activities; however, the position may also support broader project management responsibilities across R&D as business needs evolve. This role helps scope, contract ...

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$41K

$106K

$139K

How much do contract dmpk jobs pay per year?

As of Aug 22, 2026, the average yearly pay for contract dmpk in the United States is $106,034.00, according to ZipRecruiter salary data. Most workers in this role earn between $89,000.00 and $119,000.00 per year, depending on experience, location, and employer.

What is a contract DMPK?

Contract DMPK (Drug Metabolism and Pharmacokinetics) positions are temporary or project-based roles focused on studying how drugs are absorbed, distributed, metabolized, and excreted in the body. Professionals in these positions support pharmaceutical and biotechnology companies by conducting laboratory experiments, analyzing data, and helping optimize drug candidates. Contract roles may be full-time or part-time, and they often involve working with interdisciplinary teams to advance drug discovery and development projects.

What skills and qualifications are needed to thrive as a contract DMPK scientist?

To thrive as a Contract DMPK Scientist, you need a solid background in pharmacokinetics, drug metabolism, and analytical chemistry, typically supported by a degree in pharmaceutical sciences or a related field. Experience with laboratory instrumentation such as LC-MS/MS, data analysis software, and familiarity with regulatory guidelines (e.g., GLP, FDA) is essential. Strong problem-solving, attention to detail, and clear communication skills set top performers apart in this role. These skills ensure accurate data generation, compliance, and effective collaboration, all of which are critical for advancing drug development projects.

What are common challenges faced by contract DMPK scientists when managing multiple client projects?

Contract DMPK (Drug Metabolism and Pharmacokinetics) scientists often juggle several client projects at once, each with distinct timelines and requirements. Balancing priorities and maintaining clear communication with clients and internal teams is essential to ensure data integrity and meet deadlines. Additionally, adapting to varied study designs and regulatory expectations across projects can be demanding, requiring strong organizational skills and attention to detail. Effective project management and proactive problem-solving are key to thriving in this dynamic environment.

What is the difference between Contract Dmpk vs Contract Pharmacologist?

AspectContract DmpkContract Pharmacologist
Required CredentialsBachelor's or Master's in Pharmacology, DMPK-specific trainingBachelor's or Master's in Pharmacology or related field
Work EnvironmentLaboratories, research facilities, contract research organizations (CROs)Laboratories, research institutions, CROs
Industry UsageDrug development, pharmacokinetics studiesDrug development, pharmacodynamics, safety assessments
Common Search/ComparisonYesNo

Contract Dmpk specialists focus on pharmacokinetics and drug metabolism, while Contract Pharmacologists often work on drug effects and safety. Both roles are essential in drug development and share similar environments and credentials, but they differ in their specific focus areas within pharmacology.

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What cities are hiring for Contract Dmpk jobs?

Cities with the most Contract Dmpk job openings:

What are the most commonly searched types of Dmpk jobs?

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What states have the most Contract Dmpk jobs?

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What job categories do people searching Contract Dmpk jobs look for?

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Contract Dmpk jobs near you
Infographic showing various Contract Dmpk job openings in the United States as of August 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 85% Physical, 9% Hybrid, and 6% Remote job distribution, with an average salary of $106,034 per year, or $51 per hour.

SENIOR DIRECTOR, TOXICOLOGY

Calibr

San Diego, CA • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 3 days ago

Job description

ABOUT US:
Calibr-Skaggs Institute for Innovative Medicines was founded on the principle that the creation of new medicines can be accelerated by pairing world-class biomedical research with state-of-the-art drug discovery and development capabilities. Calibr-Skaggs is a division of Scripps Research, a first-of-its-kind, nonprofit translational research institute dedicated to creating the next generation of medicines. Scripps Research is ranked the most influential institution in the world for its impact on innovation. Our educational and training programs mold talented and committed students and postdocs into leading-edge scientists. Leveraging the unique scientific environment of Scripps Research, impacting translational sciences, Calibr-Skaggs has created a portfolio of drug candidates, and is shaping a new paradigm for advancing nonprofit biomedical research to impact patients while reinvesting in further innovative research. We expand basic knowledge in the biosciences and use these fundamental advancements to develop profound innovations that improve wellbeing. Calibr-Skaggs' drug development portfolio spans a broad range of human diseases, including cancer, autoimmunity and inflammatory diseases, metabolic and cardiovascular diseases, infectious and neglected tropical diseases, as well as age-related and degenerative diseases. If you have a passion for making a difference, this could be your opportunity to join our transformative team.
POSITION TITLE: Senior Director, Toxicology
POSITION SUMMARY:
The Senior Director of Toxicology will be the primary toxicology expert across our pipeline, driving the design, execution, and interpretation of nonclinical safety programs from early discovery through IND filing and into clinical development.
The successful candidate will integrate toxicology strategy into the broader drug development framework, working in close partnership with Chemistry, Biology, DMPK, CMC, Regulatory, and Clinical teams.
RESPONSIBILITIES AND DUTIES:
  • Design, oversee, and interpret toxicology studies across a range of modalities, including in vitro and in vivo safety assessments, to inform candidate selection, dose selection, and clinical translation.
  • Integrate nonclinical safety data across disciplines to support program decision-making, risk assessment, and go/no-go recommendations.
  • Partner cross-functionally with Chemistry, Biology, DMPK, CMC, Regulatory, and Clinical teams to ensure cohesive and efficient program advancement.
  • Serve as a key contributor to IND filings, regulatory authority interactions, and overall development strategy, providing expert interpretation of safety data in the context of regulatory expectations.
  • Oversee and manage multiple contract research organizations (CROs) supporting outsourced toxicology studies, ensuring scientific quality, adherence to timelines, and budget accountability.
  • Stay current with evolving regulatory guidance, scientific literature, and industry best practices in nonclinical safety and toxicology.
  • Represent the toxicology function in internal program team meetings, governance reviews, and external partner
  • Details of established essential functions for this position will be addressed/discussed during the interview process.

POSITION REQUIREMENTS:
  • PhD. in Pharmacology, Toxicology, Pharmaceutical Sciences, Cell Biology, or a closely related field.
  • Diplomate of the American Board of Toxicology (DABT) certification
  • 10+ years of experience in a pharmaceutical or biotechnology industry setting, with demonstrated expertise across early- to late-stage drug development.
  • Deep understanding of regulatory expectations for preclinical development, including IND submission requirements and global regulatory agency standards (FDA, EMA, ICH).
  • Strong working knowledge of GLP regulations and their application in preclinical and early clinical
  • Proven experience managing multiple CROs and outsourced toxicology programs
  • Track record of successfully contributing to IND filings and regulatory
  • Excellent communication skills with the ability to distill complex toxicology data for cross-functional and executive
  • Experience with diverse therapeutic modalities (small molecules, biologics, or other emerging platforms).
  • Experience authoring or contributing to regulatory submissions for IND and beyond

COMPREHENSIVE BENEFITS INCLUDE:
  • Eligible for both Short-Term (STIP) and Long-Term (LTIP) Incentive Bonus programs, offering a highly competitive total rewards package.
  • Employer Contributed Retirement Plan - Depending on eligibility, employees receive an employer contributed retirement plan (no employee contribution required) and the option to contribute to a 403(b) (which is similar to a 401(k) using your own pre or post-tax dollars)
  • Full Suite of Health and Welfare plans including three medical plan options (including an HSA available option), dental, vision, life insurance, disability, EAP and more
  • Access to Flexible Spending Accounts (Medical/Dependent Care)
  • Competitive vacation and sick leave policies
  • Free, on-site parking

COMPENSATION:
The expected hiring range for this position is $230,000 TO $280,000/annually per year, commensurate with experience. Consideration will be given to experience that exceeds the listed requirements.
The above statements describe the level of work performed and expected in general terms. The statements are not intended to list all the responsibilities, duties and/or skills required of employees so classified, and the content herein is subject to change due to the business needs of Scripps Research, with or without notice. Furthermore, nothing in this job description shall be interpreted to be in conflict with or to eliminate or modify in any way the employment-at-will status of Scripps Research staff.
EEO Statement:
The Scripps Research Institute is an Equal Opportunity Employer. We promote diversity of thought, culture, and background in the fields of science. All qualified applicants are encouraged to apply and will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other legally protected characteristic or status.
Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.
For further information, please review the Know Your Rights notice from the Department of Labor.

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