South San Francisco
California, United States of America
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
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.
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.
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.
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.
These are our stories - stories of the obstacles and opportunities that define and celebrate the unique people at Genentech.