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Remote Pbpk Modeling Jobs (NOW HIRING)

Allucent

Director, Clinical Pharmacology

Cary, NC · Remote

... PK, PBPK, and QSP modeling. * Oversee the development of statistical and PK analysis plans ... Opportunity for remote/hybrid* working depending on location * Leadership and mentoring ...

Allucent

Director, Clinical Pharmacology

Cary, NC · On-site +1

... PK, PBPK, and QSP modeling. * Oversee the development of statistical and PK analysis plans ... Opportunity for remote/hybrid* working depending on location * Leadership and mentoring ...

Allucent

Director, Clinical Pharmacology

Cary, NC · Remote

... PK, PBPK, and QSP modeling. * Oversee the development of statistical and PK analysis plans ... Opportunity for remote/hybrid* working depending on location * Leadership and mentoring ...

Arvinas

DMPK Scientist

New Haven, CT · On-site +1

... New Haven, CT or a remote role based within the U.S. Principal Responsibilities Key ... drug interaction, PBPK or PK/PD modeling, human PK prediction. * General knowledge of drug ...

Arvinas

... in New Haven, CT or a remote role based within the U.S.Principal ResponsibilitiesKey ... PBPK or PK/PD modeling, human PK prediction.General knowledge of drug discovery and development ...

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How much do remote pbpk modeling jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for remote pbpk modeling in the United States is $40.33, according to ZipRecruiter salary data. Most workers in this role earn between $31.25 and $43.51 per hour, depending on experience, location, and employer.

What is the difference between Remote Pbpk Modeling vs Remote Pharmacometric Modeling?

AspectRemote Pbpk ModelingRemote Pharmacometric Modeling
Required CredentialsPhD or MSc in Pharmacology, Pharmaceutical Sciences, or related fields; experience with PBPK softwarePhD or MSc in Pharmacology, Biostatistics, or related fields; experience with pharmacometric tools
Work EnvironmentCollaborative teams in pharma/biotech companies, often remote or hybridResearch-focused settings in pharma/biotech, frequently remote
Industry UsageUsed for predicting drug absorption, distribution, metabolism, and excretion (ADME)Used for dose optimization, clinical trial simulation, and PK/PD analysis

Remote Pbpk Modeling and Remote Pharmacometric Modeling share similar credentials and work environments but focus on different aspects of drug development. Pbpk modeling emphasizes predicting ADME processes, while pharmacometric modeling concentrates on dose-response relationships. Both roles are vital in pharmaceutical research and often overlap in multidisciplinary teams.

What is remote PBPK modeling?

Remote PBPK modeling refers to performing physiologically based pharmacokinetic (PBPK) modeling tasks from a remote location, often using specialized software and secure data connections. PBPK modeling is a computational approach used in drug development to predict the absorption, distribution, metabolism, and excretion of drugs in humans and animals. Working remotely, PBPK modelers analyze data, build models, and collaborate with interdisciplinary teams, often for pharmaceutical or regulatory organizations. This role requires strong computational skills, knowledge of pharmacokinetics, and familiarity with relevant simulation software.

What are some common challenges faced by remote PBPK modeling professionals, and how can they be addressed?

Remote PBPK (Physiologically Based Pharmacokinetic) modeling professionals often encounter challenges related to effective communication and collaboration, as much of the work involves iterative discussions with cross-functional teams such as pharmacologists, clinicians, and regulatory specialists. To overcome these hurdles, utilizing robust project management tools, maintaining clear documentation, and scheduling regular virtual meetings are essential. Additionally, proactively seeking feedback and sharing interim results can help ensure alignment and maintain project momentum, despite working remotely.

What are the key skills and qualifications needed to thrive as a Remote PBPK (Physiologically Based Pharmacokinetic) Modeler, and why are they important?

To thrive as a Remote PBPK Modeler, you need a solid background in pharmacokinetics, mathematical modeling, and a relevant advanced degree such as a PhD or MS in pharmaceutical sciences or a related field. Expertise in PBPK modeling software (e.g., Simcyp, GastroPlus), programming languages (e.g., R, MATLAB), and familiarity with regulatory guidelines are typically required. Strong analytical thinking, effective communication, and self-motivation are standout soft skills in this remote role. These competencies are essential for producing accurate predictive models, meeting regulatory standards, and collaborating efficiently with cross-functional teams in a virtual environment.
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Remote Pbpk Modeling jobs near you
Infographic showing various Remote Pbpk Modeling job openings in the United States as of May 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $83,896 per year, or $40.3 per hour.
Associate Director, Clinical Pharmacology

Associate Director, Clinical Pharmacology

Enliven Therapeutics

Remote

$185K - $215K/yr

Full-time

Posted 25 days ago

Job description

Job Type
Full-time
Description
Position Title: Associate Director, Clinical Pharmacology
Job Status: Exempt, Full Time
Location: Remote
Department: Clinical Pharmacology
Company Overview
Enliven Therapeutics is a clinical-stage biopharmaceutical company focused on the discovery and development of small molecule inhibitors to help people with cancer not only live longer but live better. The Company aims to address existing and emerging unmet needs with a precision oncology approach that improves survival and enhances overall well-being. Its discovery process combines deep insights in clinically validated biological targets and differentiated chemistry with the goal of designing therapies for unmet needs.
Role Summary
The Associate Director, Clinical pharmacology, is responsible for providing clinical pharmacology input in early and late-stage clinical development. The AD will represent clinical pharmacology function in clinical study teams, provide clinical pharmacology input on the dose, PK, DDI, and other related elements of early and late-stage clinical trials, and provide guidance on CP related issues during clinical trial execution. The AD will participate in the study design and execution of clinical pharmacology studies, such as human ADME, special population PKPD, and drug-drug interaction studies. The AD will contribute to the preparation of the regulatory documents such as briefing books for regulatory meetings, INDs, and IMPD dossiers, protocols, and clinical study reports. The AD will closely collaborate with other development-functions (Toxicology, Bioanalytical, Non-clinical PK/PD, Biomarkers, Biostatistics and Data Management, Clinical Operations, and Clinical Development) to bring drug candidates from IND stage to NDA. The clinical pharmacologist should have sound knowledge on small molecular ADME. Applicants who have sound modeling and simulation experience, but no DMPK experience, are also welcome. It is preferable to have hands-on modeling experience with PBPK modeling, popPK, or PKPD modeling, but not a strict requirement.
Core Role Responsibilities:
  • Responsible for the preparation of the clinical pharmacology sections of early and late-stage clinical protocols
  • Contribute to the preparation of the IND, IB and IMPD documents
  • Be able to conduct noncompartmental PK analysis based on preliminary data using standard industry data analysis software
  • Contribute to the design of early phase clinical trials (FIH to POC)
  • Contract and monitor CRO for clinical pharmacology projects, such as popPKPD analysis, clinical pharmacology studies
  • Represents the Clin Pharm function in project teams
  • Provide clinical pharmacology input and collaborate across all areas of drug development, along with research, preclinical, bioanalytical and clinical development functions.

Requirements
  • PhD with More than 3 years (or MS with more than 6 years) of industry experience in supporting pharmacokinetics, pharmacodynamics and other clinical pharmacology components of early clinical trials within the pharmaceutical or biotech industry.
  • Experience with small molecule drug development is required. Knowledge of oncology drug development is a plus.
  • Hands on knowledge of PK/PD and statistical analyses methods used in analyzing early clinical phase data
  • Knowledge of general regulatory process and experience in writing Clin Pharm documents to support IND, EOP1, EOP2, or pre-BLA/NDA meetings with the FDA, EMA and other regulatory agencies
  • Excellent written and oral communication skills including good presentation skills
  • Hands-on modeling experience with PBPK modeling platforms is preferable

The annual salary range Enliven reasonably and in good faith expects to pay for this position at the time of this posting is $185,000 - $215,000. The actual salary offered will be determined based on factors such as experience, qualifications, skills and expertise, geographic location, and other job-related factors permitted by law. Benefits are included and other incentives such as bonus and equity may be provided. This range is subject to change based on business needs, job scope changes, market conditions, and individual qualifications. Employees and applicants may request the pay range for their position or for a position to which they are applying.
Enliven Therapeutics is proud to be an equal opportunity employer. All employment offers are contingent upon the applicant successfully completing a background screen.
Notice to agencies: Our in-house Talent Acquisition Team manages all employment opportunities at Enliven. Agencies and independent recruiters must be approved as a vendor by our HR team. To protect the interests of all parties, Enliven will not accept unsolicited resumes, profiles, or biographies. Any unsolicited submissions will be considered referrals and become the property of Enliven. Contacting hiring managers, executives, or any member of the HR team will not influence vendor approval and is strongly discouraged. Repeated outreach may impact future consideration.

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