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Contract Dmpk Jobs (NOW HIRING)

Pharmaron

Scientist II/III, LCMS Method Development

Exton, PA · On-site

$65K - $85K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Exton, PA (On-site) About Pharmaron Pharmaron is a global contract research and manufacturing ... Execute and support bioanalytical testing for DMPK and regulated studies. * Perform sample analysis ...

New

Frontage-Laboratories

Principal Scientist

Exton, PA · On-site

$120 - $160/hr

  • Medical

  • Dental

  • Life

  • Retirement

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

  • Medical

  • Dental

  • Life

  • Retirement

... 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 ...

OmicSkyBio

Be Seen First

Scientific Business Development Representative

Tampa, FL · Remote

About OmicSkyBio OmicSkyBio is a scientist-led contract research organization providing ... DMPK, PK/PD, CMC, antibodies, ADCs, recombinant proteins, or other therapeutic modalities.

New

OmicSkyBio

Be Seen First

Scientific Business Development Representative

Tampa, FL · Remote

About OmicSkyBio OmicSkyBio is a scientist-led contract research organization providing ... DMPK, PK/PD, CMC, antibodies, ADCs, recombinant proteins, or other therapeutic modalities.

New

OmicSkyBio

Be Seen First

Scientific Business Development Representative

Tampa, FL · Remote

About OmicSkyBio OmicSkyBio is a scientist-led contract research organization providing ... DMPK, PK/PD, CMC, antibodies, ADCs, recombinant proteins, or other therapeutic modalities.

New

Frontage Laboratories

Lab Technician

Exton, PA · On-site

$18.25 - $24.25/hr

  • Medical

  • Dental

  • Life

  • Retirement

... Contract Research Organization (CRO) with more than 25 state-of-the-art laboratories across the ... DMPK), pharmacodynamics (PD), bioanalytical services, safety and toxicology, Chemistry ...

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Contract Dmpk information

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$106K

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How much do contract dmpk jobs pay per year?

As of Aug 14, 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 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 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 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?

The most popular types of Dmpk jobs are:

What states have the most Contract Dmpk jobs?

States with the most job openings for Contract Dmpk jobs include:

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

The top searched job categories for Contract Dmpk jobs are:

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 87% Physical, 8% Hybrid, and 5% Remote job distribution, with an average salary of $106,034 per year, or $51 per hour.

Scientist II/III, LCMS Method Development

Pharmaron

Exton, PA • On-site

$65K - $85K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Job description

Position: Scientist II/III, LCMS Method Development
Salary Range: $65,000-$85,000
Location: Exton, PA (On-site)
About Pharmaron
Pharmaron is a global contract research and manufacturing organization (CRO/CDMO) helping pharma and biotech companies bring new therapies to life. With over 25,000 employees worldwide across 28 locations in the US, UK, China, and Singapore, we support drug discovery through to manufacturing with fully integrated high-quality services.
We're proud of the impact we make and just last year, we supported 887 discovery projects, 1,100+ CMC programs, and 1,397 clinical trials across all phases. Our teams are involved in everything from small molecules, ADC's, biologics, and gene therapies and we work with more than 3,300 global customers. To learn more, visit .
Job Overview:
Pharmaron is seeking a Scientist II/III, LCMS Method Development to join our growing Bioanalytical Sciences team in Exton, PA. In this role, you will contribute to the development and validation of innovative bioanalytical methods supporting drug discovery and development programs across a diverse range of therapeutic modalities, including small molecules, peptides, oligonucleotides, PROTACs, biologics, and emerging therapies.
Key Responsibilities
  • Independently develop, optimize, validate, and troubleshoot LC-MS/MS bioanalytical methods.
  • Design scientifically sound studies that meet sponsor and internal objectives.
  • Execute and support bioanalytical testing for DMPK and regulated studies.
  • Perform sample analysis using HPLC and LC-MS/MS platforms in compliance with developmental and GLP requirements.
  • Review and execute study protocols governing bioanalytical studies and sample analysis.
  • Process, analyze, interpret, and report study data.
  • Author protocols, validation reports, technical summaries, and study reports.
  • Support regulatory submissions through high-quality scientific documentation.
  • Serve as Principal Investigator (PI) and/or Study Director (SD) within areas of expertise.
  • Actively identify and resolve technical challenges while driving continuous improvement.
  • Collaborate with scientists, project teams, management, business development, and clients to ensure successful project execution.
  • Participate in project review meetings and compliance-related initiatives.

What We're Looking For
  • Bachelor's degree in Pharmaceutical Sciences, Chemistry, Life Sciences, or a related scientific discipline.
  • Scientist II: Minimum 2 years of bioanalytical testing experience.
  • Scientist III: Minimum 4 years of bioanalytical testing experience.
  • Experience supporting development and/or GLP-regulated bioanalytical studies.
  • Strong understanding of HPLC and LC-MS/MS methodologies.
  • Excellent analytical thinking, troubleshooting, and organizational skills.
  • Ability to thrive in a fast-paced, collaborative, and matrixed environment.

Preferred Qualifications
  • Experience with LC-MS/MS method development and validation.
  • Experience analyzing peptides, oligonucleotides, PROTACs, and complex biologics.
  • Familiarity with DMPK studies and regulated bioanalysis.
  • Experience authoring scientific reports and supporting regulatory submissions.
  • Prior CRO, pharmaceutical, or biotechnology industry experience.
  • Experience serving in client-facing scientific roles.

Why Pharmaron?
Pharmaron is a premier service provider for the life sciences industry. Founded in 2004, Pharmaron has invested in its people and facilities and established a broad spectrum of research, development, and manufacturing service capabilities throughout the entire drug discovery, preclinical, and clinical development process across multiple therapeutic modalities, including small molecules, biologics, and CGT products. With over 25,000 employees and operations in the US, UK, China, and Singapore. Pharmaron has an excellent track record in delivering R&D solutions to its partners in North America, Europe, Japan, and China.
Collaborative Culture: You will thrive in our inclusive and collaborative environment, where teamwork and innovation go hand in hand. Here, your voice matters, and your contributions make a real impact. "Employees Number One" and "Clients Centered" are the core cultural values at Pharmaron. Our culture, which sets Pharmaron apart from other organizations, has evolved from our deep commitment to our employees, partners, and collaborators.
Benefits: As part of our commitment to your well-being, we offer a comprehensive benefits package:
  • Comprehensive Medical, Dental & Vision Insurance with significant employer contributions
  • 401(k) Retirement Plan with generous employer matching
  • Generous Paid Time Off (PTO), Paid Sick Leave & Company Holidays to support work-life balance
  • Employer-funded Health Savings Account (HSA) contributions (for eligible plans), plus Healthcare & Dependent Care Flexible Spending Accounts
  • 100% Employer-paid Employee Life Insurance, AD&D, Short- and Long-Term Disability Insurance
  • Employee Assistance Program (EAP), mental health resources, and wellness programs
  • Family-friendly benefits, including fertility support and maternity resources
  • Professional development and career growth opportunities within a leading global CRO/CDMO

How to Apply:
Ready to seize this incredible opportunity? Join us at Pharmaron and be part of a dynamic team driving innovation and excellence in biopharmaceutical research and development. Apply online today!
As an Equal Employment Opportunity and Affirmative Action employer, Pharmaron values diversity and inclusion in the workplace, fostering an environment where all individuals are empowered to succeed. Join us in our mission to make a difference in the world of life sciences.
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