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Dmpk Remote Jobs (NOW HIRING)

... in New Haven, CT or a remote role based within the U.S.Principal ResponsibilitiesKey ... Serve as a project DMPK scientist and advise discovery teams on strategies for early ADMET ...

... New Haven, CT or a remote role based within the U.S. Principal Responsibilities Key ... Serve as a project DMPK scientist and advise discovery teams on strategies for early ADMET ...

You'll work closely with clinical study teams, translational teams (DMPK, Translational Modeling ... We ask that remote employees commit to regular on-site visits for routine work and departmental ...

Drug discovery (medicinal chemistry, biology, HTS, DMPK) * Preclinical / translational research (PK ... Fully remote, asynchronous work environment with flexible scheduling Additional Information

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Dmpk Remote information

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$57.5K

$191.3K

$230.5K

How much do dmpk remote jobs pay per year?

As of Jun 5, 2026, the average yearly pay for dmpk remote in the United States is $191,320.00, according to ZipRecruiter salary data. Most workers in this role earn between $135,500.00 and $229,000.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a DMPK (Drug Metabolism and Pharmacokinetics) Scientist in a remote role, and why are they important?

To excel as a DMPK Scientist remotely, you need a background in pharmacology, chemistry, or related life sciences, often supported by an advanced degree (MS/PhD) and experience in drug metabolism or pharmacokinetics. Familiarity with analytical tools such as LC-MS/MS, pharmacokinetic modeling software (e.g., Phoenix WinNonlin), and electronic lab data systems is essential. Strong communication, self-motivation, and organizational skills are crucial for effective collaboration and project management in a remote setting. These competencies ensure accurate data analysis, clear reporting, and efficient teamwork, which are critical for successful drug development.

What are some typical challenges faced by professionals in remote DMPK roles, and how can they be addressed?

Working in a remote DMPK (Drug Metabolism and Pharmacokinetics) role often involves coordinating across time zones and managing complex data sets without direct access to laboratory facilities. Key challenges include maintaining effective communication with interdisciplinary teams, ensuring data integrity, and staying updated with evolving regulatory standards. To address these, professionals should leverage robust project management tools, establish regular virtual check-ins, and prioritize clear documentation. Proactively seeking opportunities for remote collaboration and continuous learning can also help overcome these challenges and contribute to career growth.

What are DMPK remote jobs?

DMPK (Drug Metabolism and Pharmacokinetics) remote jobs are positions that focus on studying how drugs are absorbed, distributed, metabolized, and excreted in the body, while allowing professionals to work from home or another remote location. These roles typically involve designing and analyzing experiments, interpreting pharmacokinetic data, and supporting drug development processes using specialized software and virtual collaboration tools. Remote DMPK scientists may work for pharmaceutical companies, biotech firms, or research organizations, and must have strong communication and analytical skills to collaborate effectively with in-person teams.

What is the difference between Dmpk Remote vs DMPK Scientist?

AspectDmpk RemoteDMPK Scientist
Required CredentialsBachelor's or Master's in Pharmacology, Toxicology, or related field; experience in DMPK studiesTypically requires a PhD or equivalent in Pharmacology, Pharmacokinetics, or related discipline; extensive DMPK experience
Work EnvironmentRemote, often collaborative with teams across locationsLaboratory and office-based, with some remote flexibility depending on employer
Industry UsageUsed in biotech and pharmaceutical companies for remote DMPK rolesCommonly used in research institutions and pharma companies for DMPK research

In summary, Dmpk Remote roles typically require a bachelor's or master's degree and focus on remote collaboration, while DMPK Scientist positions usually demand a PhD and involve hands-on laboratory work. Both roles are essential in drug development but differ in experience level and work setting.

More about Dmpk Remote jobs
What cities are hiring for Dmpk Remote jobs? Cities with the most Dmpk Remote 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 Dmpk Remote jobs? States with the most job openings for Dmpk Remote jobs include:
Infographic showing various Dmpk Remote job openings in the United States as of May 2026, with employment types broken down into 86% Full Time, 11% Part Time, and 3% Contract. Highlights an 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $191,320 per year, or $92 per hour.
DMPK Scientist

Full-time

Medical, Dental, Vision, Life

Posted 6 hours ago


Job description

Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its proprietary PROTAC Discovery Engine platform to engineer proteolysis targeting chimeras, or PROTAC targeted protein degraders, that are designed to harness the body's own natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins.Arvinas is currently progressing multiple investigational drugs through clinical development programs, including ARV-102, targeting LRRK2 for neurodegenerative diseases; ARV-806, targeting KRAS G12D for mutated cancers, including pancreatic, colorectal, and non-small cell lung cancers; ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; ARV-027, targeting the polyglutamine-expanded androgen receptor, or polyQ-AR, in skeletal muscle; and vepdegestrant, targeting the estrogen receptor for patients with locally advanced or metastatic ER+/HER2- breast cancer.On August 8th 2025, the U.S. Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an investigational, orally bioavailable PROTAC estrogen receptor degrader- for its use as a monotherapy in the treatment of adults with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-), ESR1-mutated advanced or metastatic breast cancer previously treated with endocrine-based therapy.

In September 2025, Arvinas and Pfizer announced their plan to jointly select a third party for the out-licensing and commercialization of vepdegestrant.In April 2024, Arvinas entered into a transaction with Novartis, including a global license agreement for the development and commercialization of the clinical stage PROTAC androgen receptor protein degrader ARV-766 for the treatment of prostate cancer. The transaction closed in May 2024.#TeamArvinas is made up of passionate and curious employees, whose diverse thoughts and perspectives are highly valued. Arvinas employees embrace the freedom to pursue innovation, think creatively, and give back.

They are driven by the company's values and mission - to improve the lives of patients with serious diseases by pioneering therapies created with our revolutionary PROTAC protein degradation platform. We're really excited about the work we're doing inside and outside of Arvinas, and think you will be, too. But don't just take our word for it - learn more about life at Arvinas and what employees have to say.Arvinas is headquartered in New Haven, Connecticut.

For more information about Arvinas, please visit www.arvinas.com and connect on LinkedIn and X.Position Summary We have an exciting opening for an experienced DMPK scientist. The incumbent will contribute as a DMPK scientist on project teams from drug discovery through all stages of drug development, with a scientific background on key aspects of DMPK science, including but not limited to in vitro and in vivo ADME, animal PK, toxicokinetics, drug metabolism, DME- and transporter-based DDI, 14C-ADME studies, QWBA, human PK prediction. This position reports to the Head of Nonclinical Sciences and may be based at our headquarter location in New Haven, CT or a remote role based within the U.S.Principal ResponsibilitiesKey responsibilities of this role include, but are not limited to:Serve as a project DMPK scientist and advise discovery teams on strategies for early ADMET profiling up to the selection of lead candidate into preclinical development.Represent DMPK function on company-wide development teams to support the advancement of preclinical and clinical development assets.Contribute to the in vitro DDI and other in vitro/in vivo DMPK assessment for individual preclinical drug candidates and ensure timely availability of key data as part of the IND enabling activities.Recommend stage appropriate clinical DDI strategy to the clinical pharmacology function.

Contribute to outsource of DMPK studies and ensure timely and high quality conduct of in vitro and in vivo ADMET studies. Partner with key CROs to develop and customize ADMET assays to support PROTAC drug discovery and development.Contribute to the preparation of DMPK component of regulatory documents such as IND, IB, or other documents.Stay up to date with the scientific advance and regulatory landscape for DMPK science in drug discovery and developmentQualificationsIn-depth knowledge or expertise on one or several aspects of DMPK science in drug discovery and/or development, such as biotransformation, bioanalysis, pharmacokinetics, toxicokinetics, DME- and transporter-based drug-drug interaction, PBPK or PK/PD modeling, human PK prediction.General knowledge of drug discovery and development process.Experience in representing DMPK function on discovery and development teams.Ability to integrate DMPK knowledge of individual drugs and prepare DMPK components of regulatory documents.Hands-on experience and proficiency in PK analysis with PK or modeling software such as Phoenix.Knowledge of relevant regulatory guidance in areas such as drug-drug interaction, bioanalysis, and GLP.Arvinas will not be providing VISA sponsorship for this position. You must have the ability to work without a need for a current or future VISA sponsorship.The duties of this role are generally conducted in a combination of lab and home office environments.

Employees must be able, with or without an accommodation to lift/carry 15/30 pounds unassisted/assisted; work comfortable in a controlled environment with and around biological, infectious and hazardous materials; gown/degown PPE; use a computer; engage in communications via phone, video, and electronic messaging; engage in problem solving, analysis and dialogue; collaborate with others; maintain general availability during standard business hours.Education Ph.D. in pharmaceutical science, chemistry, biochemistry, or related scientific discipline with ten-plus years of relevant experience in DMPK in the biopharmaceutical industry or CROs supporting pharmaceutical development, preferably with a focus on small molecules.Direct experience with PROTAC, molecular glue, or ADC highly desirable.Arvinas is proud to offer a competitive package of base and incentive compensation as well as a comprehensive benefits program designed to support the health, wellness and financial security of our employees and their families. Benefits include group medical, vision and dental coverage, group and supplemental life insurance, and much more.

To learn more about Arvinas, please visit www.arvinas.com Arvinas is an equal opportunity employer. All qualified applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identify, national origin, disability or protected veteran status. Salary: . Date posted: 05/06/2026