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How much do dmpk jobs pay per year?

As of Aug 22, 2026, the average yearly pay for dmpk in Delaware is $191,485.00, according to ZipRecruiter salary data. Most workers in this role earn between $135,600.00 and $229,200.00 per year, depending on experience, location, and employer.

What is a DMPK?

A DMPK (Drug Metabolism and Pharmacokinetics) job involves studying how drugs are absorbed, distributed, metabolized, and excreted in the body. Professionals in this field assess drug interactions, optimize dosing strategies, and predict potential toxicity. They work closely with medicinal chemists, pharmacologists, and toxicologists to support drug discovery and development. DMPK scientists use analytical techniques such as mass spectrometry and in vitro/in vivo models to evaluate pharmacokinetic properties. Their work helps ensure the safety and efficacy of new therapeutics before clinical trials.

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

To succeed in a DMPK (Drug Metabolism and Pharmacokinetics) role, you generally need advanced knowledge in pharmacology, biochemistry, and analytical chemistry, supported by a relevant advanced degree such as an MSc or PhD. Familiarity and hands-on experience with LC-MS/MS instrumentation, pharmacokinetic modeling software (such as Phoenix WinNonlin), and regulatory guidelines are highly valuable. Strong critical thinking, communication, and organizational skills help distinguish candidates, especially when interpreting data and collaborating with multidisciplinary teams. Mastery of these skills is essential for ensuring effective evaluation of drug candidates and clear communication of findings in a fast-paced research environment.

What are some typical challenges faced in a DMPK position and how are they addressed?

Professionals in DMPK roles often encounter the challenge of interpreting complex pharmacokinetic and metabolism data under tight project timelines. Coordinating data from various sources, troubleshooting analytical equipment, and keeping pace with evolving regulatory standards can demand adaptability and proactive problem-solving. Effective DMPK scientists collaborate closely with medicinal chemists, toxicologists, and clinical teams to ensure integrated drug development efforts. Many teams also have robust mentorship and training in place to help new hires navigate technical hurdles and develop their expertise. Overcoming these challenges requires a combination of technical rigor, teamwork, and ongoing professional development.

What are the most commonly searched types of Dmpk jobs in Delaware?

The most popular types of Dmpk jobs in Delaware are:

What are popular job titles related to Dmpk jobs in Delaware?

For Dmpk jobs in Delaware, the most frequently searched job titles are:

What job categories do people searching Dmpk jobs in Delaware look for?

The top searched job categories for Dmpk jobs in Delaware are:

What cities in Delaware are hiring for Dmpk jobs?

Cities in Delaware with the most Dmpk job openings:

Dmpk jobs near you
Infographic showing various Dmpk job openings in Delaware as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution, with an average salary of $191,485 per year, or $92.1 per hour.

Research Scientist (Sample Analysis) - Bioanalytical Dept

QPS, LLC

Newark, DE • On-site

$88K - $98K/yr

Full-time

Life, Retirement

Posted 18 days ago

Job description

Do you want to be part of an organization that is making a difference in the lives of millions of people worldwide? If so, we want to hear from you! QPS, LLC has an opening for a Research Scientist in our Bioanalytical (GBA) department. GBA is comprised of three laboratory operation unit: Small Molecules, Proteins, and Oligonucleotides, and each unit has their own Method Development/Method Validation/Sample Analysis (MD/MV/SA) group. In this role, you will play a pivotal part in QPS’ continued expansion of our bioanalytical capabilities to support drug development of small molecules, antibody drug conjugate, protein, and genetic medicines.


The GBA department expertise lies in the quantitation of small molecules, peptides, proteins, oligonucleotides, and biomarkers by various chromatographic (standard flow LC, microflow LC, SFC) couple to tandem mass spectrometric (MS/MS, MS/HRMS, hybrid/immunocapture mass spec) techniques. We have been pivotal in supporting most of the HIV drugs, most of the HBV/HCV drugs, 2 of the 15 ADCs, and 7 of the 24 oligonucleotides therapeutics approved by FDA/EMA.


We are currently looking for Research Scientists for our Sample Analysis groups. This position will serve as Principal Investigator (PI) on Bioanalytical studies and be responsible for study management, interpretation and reporting of study data, and in concert with team members and peers, will participate in method validation when needed


QPS’ Story:

Since its inception, QPS has been assisting pharmaceutical, biotechnology and medical device companies with their drug development efforts by providing a full range of Neuropharmacology, DMPK, Toxicology, Bioanalysis, Translational Medicine, Early Phase Clinical and Phase II – IV Clinical Research services. To meet the needs of our clients, we strive to employ talented, caring and committed individuals who will work collaboratively towards achieving our mission of improving human health and the quality of life.


Team members enjoy challenging and rewarding work, and are encouraged achieve their best. Underpinning the operation is a culture that values diversity, innovation, accountability, team work and a friendly atmosphere where performance is recognized and rewarded. We provide unique company benefits, training, and advancement opportunities. Most importantly, we value each of our team members as employees and as individuals.


If this sounds like your ideal work environment, then we would love to speak with you, so apply today!


Please visit our website (www.qps.com) for more information and to see all current openings.


The Job

  • Independently manage multiple sample analysis projects/studies at the same time with minimum supervision.
  • Prepare, and/or review and understand study protocols.
  • Coordinate with client and internal resources to plan, design and conduct studies
  • Evaluate significance of data and report findings.
  • Prepare Study summaries and/or reports.
  • Set-up, utilize, and maintain complex instrumentation
  • Communicate project timelines, status, data, reports, and inquiries to client and/or study sites, effectively addressing any issues that may arise.
  • Maintain the proper level of regulatory compliance for each study, preparing QA related documents and addressing QA audit findings.
  • Maintain schedule of projects and timelines.
  • Supervise, train and/or mentor junior scientific staff
  • Develop, validate and run sensitive, reliable and efficient LC/MS/MS assays for TK/PK assessment.
  • Ensure that GLP regulations and SOPs are followed in all bioanalytical service activities.


Work Location

  • This job will be 100% QPS-office/facility based


Requirements

The successful candidate will hold an advanced degree in Analytical Chemistry, Biochemistry, Pharmacology, or related scientific discipline:

  • Ph.D. degree
    • Recent graduates must have with direct experience on LC-MS/MS analysis
    • If more than 2 years since graduation, candidates must have direct experience on method development of bioanalytical assays using LC-MS/MS, particularly having CRO experience
  • Understanding of experimental design and planning, and data collection and analysis software.


Why You Should Apply

  • Great learning opportunities, especially for those new to the field. Our seasoned professionals are here to support and work with you to explore your learning potential and career goals.
  • Structured Career Ladders that provide excellent growth based on your personal aspirations.
  • Bonuses and merit increases are a part of the QPS total rewards approach and are linked to individual, team and company performance.
  • Solid Benefits package, including Company-matched 401(k), and Company-sponsored Group Life/AD&D and Short and Long-term Disability Insurance
  • Park-like setting in Newark, Delaware
  • Internal committees designed with the needs and enjoyment of QPS employees in mind.


QPS, LLC is an Equal Employment Opportunity/Affirmative Action Employer. In accordance with federal, state, and local laws, we recruit, hire, promote and evaluate all personnel without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, citizenship status, physical disability, protected veteran status, or any other characteristic protected by law. Job applicants and present employees are evaluated solely on ability, experience, and the requirements of the job. In addition, QPS, LLC is a federal contractor and desires priority referrals of protected veterans.