2026 Summer Intern - Early Phase Biometrics Data Management
Department Summary
This role is in Early Development Biometrics (EDB), a core function within Product Development Data Sciences (PDD) that provides strategic leadership and scientific rigor across early clinical development at Roche. We partner across Biostatistics, Analytical Data Science, and Data Management to enable data-driven decision-making from first-in-human through proof-of-concept studies.
As trusted partners in early development, we design efficient and innovative clinical trials, apply rigorous statistical methods, and implement high-quality programming and analytical solutions to accelerate timelines, de-risk development, and increase the probability of technical success. Our integrated teams operate with agility and scientific depth, supporting exploratory analyses, early regulatory engagements, and complex data-generation needs across therapeutic areas. Together, we bring scientific rigor, technical innovation, and strategic insight to shape the future of early development and deliver better outcomes for patients.
This internship position is located in South San Francisco, on-site.
The Opportunity
Define and implement a cross-study data standard for raw inputs from Microperimetry, standard automated perimetry, and VR perimetry (file formats, metadata, naming conventions, and required fields).
Define and implement cross-study data standards for extracted outputs (e.g., sensitivity maps, global indices, pointwise measures, reliability metrics), including units, derivations, and provenance.
Build and document an end-to-end data processing workflow (ingestion → validation → transformation → standard datasets) to enable scalable reuse across existing and upcoming studies.
Collaborate with Biostatistics, Analytical Data Science, and Data Management partners to gather requirements, iterate on standards, and ensure downstream analysis compatibility.
Support exploratory analyses to demonstrate the utility of the standard (e.g., cross-sectional and longitudinal correlations between functional outcomes and OCT structure metrics), and summarize findings for stakeholders.
Program Highlights
Intensive 12 months, full-time (40 hours per week) paid internship.
Program start dates are in June 2026.
A stipend, based on location, will be provided to help alleviate costs associated with the internship.
Ownership of challenging and impactful business-critical projects.
Work with some of the most talented people in the biotechnology industry.
Who You Are
Required Education
You meet one of the following criteria:
Must be pursuing a Master's Degree (enrolled student).
Must be pursuing a PhD (enrolled student).
Required Majors: Quantitative field, including computer science, biomedical engineering, mathematics, physics etc.
Required Skills: Familiar with Python and HPC environment.
Preferred Knowledge, Skills, and Qualifications
Excellent communication, collaboration, and interpersonal skills.
Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion.
Experience working with medical tabular and imaging data.
Relocation benefits are not available for this job posting.
The expected salary range for this position based on the primary location of California is $40.00-$50.00 per hour. Actual pay will be determined based on experience, qualifications, geographic location, and other job-related factors permitted by law. This position also qualifies for paid holiday time off 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
About Genentech
We're passionate about finding solutions for people facing the world's most difficult-to-treat conditions. That is why we use cutting-edge science to create and deliver innovative medicines around the globe. To us, science is personal.
Making a difference in the lives of millions starts when you make a change in yours. If you’d like to join our team, view our openings at gene.com/careers.
Our patient resource center is dedicated to getting patients and caregivers to the right resources. You can reach them at 1 (877) GENENTECH (436-3683)
Monday-Friday, 6am-5pm PST or patientinfo@gene.com.
Community Guidelines:
1. We want to foster positive conversation around the issues we are passionate about. To that end, we remove profanity, content that contains threatening language, content that is aimed at private individuals, personal information, and repeated unwanted messages.
2. Don’t mention any medicines by name — ours or anyone else’s.
Because of the fair balance rules governing our industry, we cannot post any comments that reference any pharmaceutical brand, product, or service. Please do not mention any specific medicines by name, or include any links to third party sites in your comments.
3. This isn’t the place to report or discuss side effects.
This site is not intended as a forum for reporting side effects experienced while taking a Genentech product. Instead, you should report any side effects to Genentech Drug Safety at 1-888-835-2555. You can also report side effects of any prescription product directly to the FDA at 1-800-FDA-1088 or by visiting www.FDA.gov/medwatch.
4. Don’t pitch your product or service.
Please don't use our page as a place to promote your product or pitch your services. Please also avoid posting links to external sites. We reserve the right to remove any posts that are deemed promotional.
