Role at a glance
- Job function
-
Engineering & R&D Biotechnology & Pharmaceutical R&D
- Salary
- $120.7K – $224.1K/yr
- Location
- South San Francisco, United States
- Work arrangement
- On-site
- Employment
- Full-time
- Experience
- 0-2 years of experience of PKPD of biologics and drug development
- Education
- PhD
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Role Summary
This Senior Scientist position in the translational Pharmacokinetics and Pharmacodynamics department supports preclinical PKPD efforts for biologics in Genentech’s pipeline. The role provides technical support for assessing drug candidates and marketed products and collaborates with multiple departments across research, development, safety, and regulatory functions.
What You'll Do
- Design, conduct, analyze, and interpret in vitro and in vivo ADME and PKPD studies
- Prepare summary tables and reports for non-clinical studies and documents for regulatory agencies under supervision
- Present data at project team and department meetings and conferences
- Publish PKPD-focused research in scientific, technical, or medical journals
- Manage a laboratory program supporting basic PKPD research and pipeline projects
- Collaborate with departments including Clinical Pharmacology, Research, Bioanalytical Sciences, Safety Assessment, Regulatory Affairs,...
Generated from the employer's posting. Verify important details before applying.
View full postingQualifications
Ph.D., M.D., PharmD, or equivalent curriculum in a related discipline; 0-2 years of experience in PKPD of biologics and drug development; strong knowledge of laboratory techniques and safety; experience with quantitative PKPD software including WinNonlin, NONMEM, ADAPT II, Matlab, Simbiology, or R; independent study design, analysis, interpretation, and documentation; good communication skills.
Required
- Ph.D., M.D., PharmD degree or equivalent curriculum in pharmacology, pharmaceutical science, biology, bioengineering, chemistry,...
- 0-2 years of experience of PKPD of biologics and drug development
- Strong knowledge of laboratory techniques and safety
- Experience in quantitative PKPD software, including WinNonlin, NONMEM, ADAPT II, Matlab, Simbiology, or R
- Demonstrated independent thought and creativity in a relevant discipline
- Ability to independently design, carry out, analyze, interpret, and document studies and experiments
- Good communication skills
Original job description
Content provided by the employer
Original job description
Content provided by the employer
We advance science so that we all have more time with the people we love.
This opening will consider either a Senior Scientist position at the translational Pharmacokinetics and Pharmacodynamics (tPKPD) department at the Development Sciences division in Genentech Research and Early Development (gRED) unit.
The focus of this position is to support the preclinical pharmacokinetic and pharmacodynamics (PKPD) efforts to guide the design, delivery and development of biologics in the Genentech pipeline. Core responsibilities include providing technical support for the PKPD assessment of drug candidates and marketed products and working independently or under the direct supervision of a Scientist.
The Opportunity:
The responsibilities of this Senior Scientist project pathologist position will :
Design, conduct, analyze and interpret all in vitro and in vivo ADME and PKPD studies that are necessary to understand the pharmacology of drug candidates in animals and predict their behavior in humans
Prepare summary tables and reports for non-clinical studies; may prepare documents for regulatory agencies, including INDs and BLAs under the supervision of a Scientist
Present data at project teams and department meetings and conferences as appropriate
Publish innovative PKPD focused research in high quality scientific, technical or medical journals.
Manage an active laboratory program that supports basic research in PKPD and also supports 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, Technical Development, and others
Participate in compliance and safety related activities Perform other duties, as assigned
Who You Are:
Ph.D., or M.D., or PharmD degree or equivalent curriculum in pharmacology, pharmaceutical science, biology, bioengineering, chemistry, physiology or related disciplines is required (experience is specific to job level). Persons without formal degree who have comparable depth and breadth of training and experience (gained at GNE or elsewhere), and who meet job-specific criteria, are eligible for consideration. Post doctoral experience may not be required; 0-2 years of experience of PKPD of biologics and drug development
Outstanding record of accomplishment in his/her field as evidenced by his/her co authored publications, patents, internal reports and/or regulatory filings. .
Strong knowledge of laboratory techniques and safety is required; 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 in relevant discipline; independently designs, carries out, analyzes, interprets, and documents studies and experiments;
Good communication skills, independently presents at department and project team meeting
Relocation Assistance benefits are available for this posting.
The expected salary range for this position based on the primary location of San Franscico, CA is $ 120,700 – $224,100Annual. 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 here:
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 form Accommodations for Applicants.
About the company
Genentech
Large Enterprise
Genentech, a member of the Roche Group, is a biotechnology company focused on discovering, developing, manufacturing, and commercializing innovative medicines for patients with serious medical conditions. Founded in 1976, Genentech has played a pioneering role in the biotech industry, particularly in the development of targeted therapies for cancer and other diseases. The company is committed to advancing science and addressing unmet medical needs through cutting-edge research and collaboration, making it a leader in the field of biotechnology. With a strong emphasis on sustainability and corporate responsibility, Genentech is dedicated to improving patient outcomes and enhancing healthcare globally.