The Position
We advance science so that we all have more time with the people we love.
The Executive Director of Regulated Bioanalysis Implementation & Oversight (RBIO) provides strategic, scientific, and organizational leadership for a critical function in the BioAnalytical Sciences (BAS) organization within Genentech Early Research and Development (gRED) . RBIO enables the successful implementation of bioanalytical strategies across nonclinical and clinical development by ensuring the timely delivery of high-quality pharmacokinetic (PK), immunogenicity, and soluble biomarker data that support global regulatory submissions and advance Genentech's diverse portfolio from early development through post-marketing.
As an integral member of the BAS Leadership Team, the Executive Director is responsible for evolving RBIO's scientific, operational, and leadership capabilities to meet the needs of an increasingly complex portfolio that includes biologics, antibody-drug conjugates, nucleic acid therapeutics, and advanced modalities such as cell and gene therapies. This role combines operational excellence with strategic vision, ensuring that RBIO continues to evolve alongside advances in science, technology, regulatory expectations, and modern operational capabilities while maintaining the highest standards of scientific excellence, quality, and compliance.
The RBIO organization translates BAS scientific strategy into high-quality bioanalytical execution through strategic external partnerships, robust operational oversight, and delivery of regulated bioanalytical data supporting nonclinical and clinical development. Through its integrated capabilities in global CRO portfolio management, clinical bioanalysis operations, and quality reagent solutions, RBIO enables the generation of foundational pharmacokinetic, immunogenicity, and biomarker data while advancing operational excellence, scientific innovation, and scalable capabilities that support Genentech's increasingly complex portfolio.
The Executive Director partners closely with leaders across Research, Development Sciences, Early Clinical Development, Product Development, Clinical Pharmacology, DMPK, Translational Medicine, and the broader Roche organization to ensure RBIO delivers innovative, scalable, and efficient bioanalytical solutions that accelerate development of transformative medicines for patients. As a member of the BAS Leadership Team, this leader helps translate BAS scientific strategy into organizational capability while fostering a culture of scientific excellence, learning, innovation, and continuous improvement.
Additionally, the Executive Director will be a member of the gRED Senior Leader community working alongside their peers to support enterprise-wide organizational strategies and change management initiatives.
The Opportunity:
The Executive Director is responsible for the strategic, scientific, operational, and organizational leadership of RBIO, including but not limited to:
As an integral member of this dynamic team, you will :
Strategic Leadership
Scientific and Operational Excellence
External Partnerships and Enterprise Influence
Organizational Leadership
Portfolio Delivery and Governance
Who You Are:
BS, MS, MBA, PhD, or equivalent degree in Biological Sciences, Chemistry, or a related discipline with 15+ years of relevant pharmaceutical or biotechnology industry experience supporting drug development and bioanalytical sciences, including significant leadership experience leading complex scientific and operational organizations across multiple organizational levels and influencing outcomes within a highly matrixed global environment.
Extensive experience providing scientific and operational leadership for regulated bioanalysis supporting pharmacokinetic, immunogenicity, and biomarker strategies across all phases of drug development.
Extensive experience developing and executing global bioanalytical outsourcing strategies, establishing and managing strategic CRO partnerships, and ensuring delivery of high-quality regulated bioanalytical studies w/extensive experience partnering with global clinical study teams and overseeing regulated bioanalytical deliverables, including technical oversight, operational execution, and delivery of clinical study milestones.
Demonstrated scientific leadership supporting diverse therapeutic modalities, including biologics, antibody-drug conjugates, nucleic acid therapeutics, and emerging modalities such as cell and gene therapies.
Deep understanding of global regulatory requirements governing bioanalytical sciences, GxP compliance, sponsor oversight, quality systems, and regulated bioanalytical sample analysis.
Demonstrated ability to anticipate future scientific and operational needs while building organizational capabilities that support evolving portfolio requirements and emerging technologies. Experience evaluating and implementing innovative operating models, automation, connected data solutions, and AI-enabled approaches that improve scientific insight, operational performance, and organizational capability.
Proven ability to influence scientific and operational strategy while building strong partnerships across highly matrixed global organizations and external collaborators. Strong business acumen with demonstrated experience managing organizational budgets, resources, external partnerships, portfolio priorities, and long-term operational planning.
Outstanding communication, collaboration, and influencing skills with demonstrated ability to engage scientific, operational, and executive stakeholders and effectively lead through influence in a highly matrixed global environment w/proven track record of developing leaders, building high-performing organizations, driving organizational change, fostering succession planning, and creating an inclusive culture of scientific excellence, continuous learning, collaboration, and innovation.
Relocation benefits are available for this posting.
The expected salary range for this position based on the primary location of California is $254,500 -$472,700. 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 form Accommodations for Applicants.
| Location | South San Francisco, CA |
| Salary | $254,500–$472,700 Per Year |
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