Senior Scientist (Drug Metabolism & Pharmacokinetics)

Genentech
Genentech logo
Location
South San Francisco
Job Type
Full-time
Posted
August 23, 2026
Views
2

Job Description

The Drug Metabolism & Pharmacokinetics (DMPK) department at Genentech is seeking a highly motivated leader who will be supporting small molecule projects in discovery and development.

The DMPK group is dedicated to enabling the discovery, development and commercialization of safe and effective medicines by elucidating the absorption, distribution, metabolism, excretion and pharmacokinetic properties of traditional small molecule and emerging modality drug candidates. We accomplish this through the application of state-of-the-art technologies and sciences of bioanalysis, drug metabolism, drug transport and pharmacokinetics. The DMPK group works in close partnership with disciplines such as medicinal chemistry, pharmacology, toxicology, pharmaceutical sciences, clinical pharmacology and regulatory to optimize leads, select clinical candidates, conduct preclinical development studies, support clinical evaluation and contribute to IND and NDA filings.

The Opportunity

The individual would lead the DMPK strategy, design and oversee non-clinical studies in a highly collaborative project team environment. Specifically, the individual will be involved in the following activities as part of their role:

  • Serve as the DMPK representative on multidisciplinary project teams and communicate recommendations to project teams.

  • Lead DMPK strategy and author or review relevant sections of regulatory briefing packages/filings.

  • Design, oversee, interpret and integrate in vitro and in vivo ADME, PK and translate nonclinical data into human PK and dose predictions.

  • Identify DMPK-related risks, and develop mitigation strategies.

Who You Are

  • PhD in pharmacokinetics, drug metabolism, pharmaceutical sciences or related discipline.

  • At least 2 years of relevant pharmaceutical industry experience as a DMPK project leader.

  • Strong knowledge of ADME, PK, and the integration of DMPK data into discovery and development decisions.

  • Experience designing, interpreting and integrating nonclinical DMPK studies.

  • Ability to communicate complex scientific data, uncertainties and recommendations clearly to multidisciplinary teams and senior stakeholders.

Preferred

  • Experience as a member/leader of multi-functional project teams supporting diverse modalities (small/large molecules, peptides, degraders, conjugates etc.), in particular, those outside Lipinski’s Rule-of-5.

  • Experience supporting programs through candidate selection, IND-enabling development, clinical development or regulatory interactions.

  • Hands-on experience with PK/PD modeling and/or PBPK modeling using relevant modeling and simulation platforms are highly desired.

Together, we’ll advance along the whole patient journey with the aspiration to prevent, stop and cure diseases.

This position does offer domestic relocation.

The expected salary range for this position based on the primary location of San Francisco, CA is 124,300.00 - 230,900.00 USD. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

This position also qualifies for the benefits detailed at the link provided below.

Benefits

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

The Drug Metabolism & Pharmacokinetics (DMPK) department at Genentech is seeking a highly motivated leader who will be supporting small molecule projects in discovery and development.

The DMPK group is dedicated to enabling the discovery, development and commercialization of safe and effective medicines by elucidating the absorption, distribution, metabolism, excretion and pharmacokinetic properties of traditional small molecule and emerging modality drug candidates. We accomplish this through the application of state-of-the-art technologies and sciences of bioanalysis, drug metabolism, drug transport and pharmacokinetics. The DMPK group works in close partnership with disciplines such as medicinal chemistry, pharmacology, toxicology, pharmaceutical sciences, clinical pharmacology and regulatory to optimize leads, select clinical candidates, conduct preclinical development studies, support clinical evaluation and contribute to IND and NDA filings.

The Opportunity

The individual would lead the DMPK strategy, design and oversee non-clinical studies in a highly collaborative project team environment. Specifically, the individual will be involved in the following activities as part of their role:

  • Serve as the DMPK representative on multidisciplinary project teams and communicate recommendations to project teams.

  • Lead DMPK strategy and author or review relevant sections of regulatory briefing packages/filings.

  • Design, oversee, interpret and integrate in vitro and in vivo ADME, PK and translate nonclinical data into human PK and dose predictions.

  • Identify DMPK-related risks, and develop mitigation strategies.

Who You Are

  • PhD in pharmacokinetics, drug metabolism, pharmaceutical sciences or related discipline.

  • At least 2 years of relevant pharmaceutical industry experience as a DMPK project leader.

  • Strong knowledge of ADME, PK, and the integration of DMPK data into discovery and development decisions.

  • Experience designing, interpreting and integrating nonclinical DMPK studies.

  • Ability to communicate complex scientific data, uncertainties and recommendations clearly to multidisciplinary teams and senior stakeholders.

Preferred

  • Experience as a member/leader of multi-functional project teams supporting diverse modalities (small/large molecules, peptides, degraders, conjugates etc.), in particular, those outside Lipinski’s Rule-of-5.

  • Experience supporting programs through candidate selection, IND-enabling development, clinical development or regulatory interactions.

  • Hands-on experience with PK/PD modeling and/or PBPK modeling using relevant modeling and simulation platforms are highly desired.

Together, we’ll advance along the whole patient journey with the aspiration to prevent, stop and cure diseases.

This position does offer domestic relocation.

The expected salary range for this position based on the primary location of San Francisco, CA is 124,300.00 - 230,900.00 USD. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. A discretionary annual bonus may be available based on individual and Company performance.

This position also qualifies for the benefits detailed at the link provided below.

Benefits

Genentech is an equal opportunity employer. It is our policy and practice to employ, promote, and otherwise treat any and all employees and applicants on the basis of merit, qualifications, and competence. The company's policy prohibits unlawful discrimination, including but not limited to, discrimination on the basis of Protected Veteran status, individuals with disabilities status, and consistent with all federal, state, or local laws.

If you have a disability and need an accommodation in relation to the online application process, please contact us by completing this formAccommodations for Applicants.

Researching Genentech before you apply?

See 74 open roles · Verified H-1B salary data · Clinical-trial hiring momentum · Culture, benefits & locations.

View Genentech profile

Frequently Asked Questions

Where is the job located, and is it remote/hybrid/on-site?
The position is located in South San Francisco. The job posting does not specify a remote or hybrid work-mode policy.
What are the required qualifications and experience level for this role?
You must have a PhD in pharmacokinetics, drug metabolism, pharmaceutical sciences, or a related discipline. Additionally, you need at least 2 years of relevant pharmaceutical industry experience as a DMPK project leader, strong knowledge of ADME and PK, and experience designing and integrating nonclinical DMPK studies.
What are the key responsibilities of the Senior Scientist?
You will serve as the DMPK representative on multidisciplinary teams, lead DMPK strategy, and author or review regulatory filings. You will also design, oversee, and interpret in vitro and in vivo ADME and PK studies, translate nonclinical data into human PK and dose predictions, and identify and mitigate DMPK-related risks.
What is the salary range for this position?
The expected salary range for this position is $124,300.00 - $230,900.00 USD. Actual pay is determined by experience, qualifications, location, and other job-related factors. A discretionary annual bonus may also be available based on performance.
Does this position offer relocation support?
Yes, this position does offer domestic relocation support.

Ready to Apply?

Apply for this Position

You'll be redirected to the company's application page

Share this job:

Explore Genentech

Research the company before you apply.

  • 74 open roles
  • Verified H-1B salary data
  • Clinical-trial hiring momentum
  • Culture, benefits & locations
View company profile

Job Information

Source: workday
AI Relevance: 45/100 (Somewhat related)
Remote Type: onsite
Allowed Locations: South San Francisco
Skills & Tags:
genentech pharma

Get Similar Jobs by Email

Weekly digest of Genentech and similar companies. Free.

Related Jobs

Apply for this Position

Get weekly job alerts