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Senior Scientist, Clinical Pharmacology

South San Francisco
California, United States of America


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The Position

The Position

The Clinical Pharmacology Scientist is responsible for the Clinical Pharmacology (CP)

strategy for his/her development project[s] in order to ensure that appropriate

dose/route/schedule decisions are made for the patients. The CP Scientist uses state of the

art model-informed drug development strategies that are aligned with project needs. The CP

Scientist works in close partnership with Pharmacometricians, Biostatisticians, Clinicians and

cross-functional project teams. Responsibilities include; leading the design & review of CP

study protocols and analysis plans where appropriate, contributing to the design and review

of clinical protocols and analysis plans, analysis and interpretation of PK/PD data,

preparation and review of clinical study reports, presentation of PK/PD data at cross-functional teams, department meetings, conferences and regulatory meetings as well as

planning, implementation and organization of regulatory filings (eg. IND, End-of Phase 2

meeting, EU Scientific Advice meeting, BLA, NDA, sNDA). Performs other duties as

assigned.

Technical Skills:

Familiarity with quantitative approaches in drug development, working knowledge of relevant

modeling software (eg. NONMEM, ADAPTII, WinNonlin, Berkeley Madonna, R, S-Plus,

SimCYP, GastroPlus) and the ability to plan, organize, and critically assess and/or perform

PK/PD data analyses. Familiarity with clinical study design options, especially for phase 1

and 2 studies. Working knowledge of statistical approaches as they apply to clinical study

design & analysis. Working knowledge of relevant disease areas.

Communication Skills:

The CP Scientist requires excellent communication skills, both written and oral, in order to

deliver high quality protocols, regulatory documents, documents for team and management review, scientific manuscripts & posters for publication.

Drug Development Knowledge:

The CP Scientist requires relevant experience/knowledge of how CP science can impact

drug development. CP Scientist should have a good knowledge of GCP and working

knowledge of relevant regulatory guidelines.

Leadership:

Based on experience and ability, the CP Scientist may lead CP teams, project sub-teams

and represent CP at cross-functional project teams. Based on experience and ability, the CP

Scientist may manage other Scientists or Research Associates within CP department.

Qualifications:

  • MD, PhD, PharmD or equivalent
  • Multiple levels based on relevant experience in Pharmacokinetics, Pharmaceutical Sciences, Biomedical Engineering or related quantitative discipline.
    • Associate Scientist 0-3 years of experience
    • Scientist 3-5 years of experience
    • Senior Scientist 6-8 years of experience

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Who We Are

A member of the Roche Group, Genentech has been at the forefront of the biotechnology industry for more than 40 years, using human genetic information to develop novel medicines for serious and life-threatening diseases. Genentech has multiple therapies on the market for cancer & other serious illnesses. Please take this opportunity to learn about Genentech where we believe that our employees are our most important asset & are dedicated to remaining a great place to work.

The next step is yours. To apply today, click on the "Apply online" button.

Genentech is an equal opportunity employer & prohibits unlawful discrimination based on race, color, religion, gender, sexual orientation, gender identity/expression, national origin/ancestry, age, disability, marital & veteran status. For more information about equal employment opportunity, visit our Genentech Careers page.


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