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About the Role
This position supports preclinical pharmacokinetic and pharmacodynamics (PKPD) efforts to guide the design, delivery, and development of biologics in the Genentech pipeline. The role involves providing technical support for PKPD assessment of drug candidates and marketed products, working independently or under supervision.
Responsibilities
- Design, conduct, analyze, and interpret in vitro and in vivo ADME and PKPD studies.
- Prepare summary tables and reports for non-clinical studies.
- Prepare documents for regulatory agencies, including INDs and BLAs under supervision.
- Present data at project teams, department meetings, and conferences.
- Publish innovative PKPD focused research.
- Manage an active laboratory program supporting basic research and pipeline projects.
- Collaborate with other departments such as Clinical Pharmacology, Research, Bioanalytical Sciences, Safety Assessment, PD Biomarker/OMNI, Antibody Engineering, Non-clinical Biostatistics, Regulatory Affairs, and Technical Development.
- Participate in compliance and safety related activities.
- Perform other duties as assigned.
Requirements
- Ph.D., M.D., or PharmD degree or equivalent in pharmacology, pharmaceutical science, biology, bioengineering, chemistry, physiology, or related disciplines.
- 1-2 years of relevant industry experience in translational PKPD/pharmacology or equivalent Postdoctoral experience is preferred.
- Outstanding record of accomplishment in his/her field as evidenced by co-authored publications, patents, internal reports, and/or regulatory filings.
- Strong knowledge of laboratory techniques and safety.
- Regular GLP and laboratory safety training is required.
- Experience in quantitative PKPD software (e.g., WinNonlin, NONMEM, ADAPT II, Matlab, Simbiology, R).
- Demonstrated independent thought and creativity; independently designs, carries out, analyzes, interprets, and documents studies and experiments.
- Good communication skills.
- Independently presents at department and project team meetings.
Skills
- Translational PKPD
- Pharmacology
- ADME studies
- PKPD studies
- Quantitative PKPD software (WinNonlin, NONMEM, ADAPT II, Matlab, Simbiology, R)
- Laboratory techniques
- Laboratory safety
- GLP
- Communication skills
- Data presentation
Location
- San Francisco, CA
Work Type
- Full-time
Experience Level
- Senior Scientist
- 1-2 years of relevant industry experience or equivalent Postdoctoral experience
Education Level
- Ph.D.
- M.D.
- PharmD
- Equivalent degree or training and experience
Salary/Compensations
- $120,700 – $224,100
Benefits
- Relocation Assistance
- Discretionary annual bonus
- Detailed benefits package available
About the Company
- Genentech advances science so that we all have more time with the people we love.
- Genentech Research and Early Development (gRED) unit.
Equal Opportunity
- 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.
- Accommodations for Applicants with disabilities are available.