2026 Summer Intern - Research and Early Clinical Development(ECD) Quality, Compliance & Clinical Capabilities (QC3) jobs in United States
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Genentech · 18 hours ago

2026 Summer Intern - Research and Early Clinical Development(ECD) Quality, Compliance & Clinical Capabilities (QC3)

Genentech is a leading biotechnology company, and they are seeking a Summer Intern for their Research and Early Clinical Development Quality, Compliance & Clinical Capabilities group. This internship offers hands-on experience in quality and compliance related to clinical trials, with opportunities to engage in impactful projects and shadow key roles within the organization.

BiotechnologyLife ScienceManufacturing
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Comp. & Benefits
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H1B Sponsor Likelynote

Responsibilities

Research and summarize industry trends for the broader group, focusing on topics relevant to clinical development (e.g., healthcare compliance, privacy, artificial intelligence, FDA guidance, ICH GCP Guidelines, and enforcement of regulations)
Interview and interact with internal and external partners to gather input for assigned projects
Contribute to the delivery of process or technical solutions that support ECD operations
Assist with project plans, establish timelines, track deliverables, assess critical dependencies, develop meeting materials, and drive action item completion
Prioritize workloads and ensure deadlines are met across various tasks
Help review study and department documents, collaborating with accountable team members to resolve inconsistencies
Develop a poster for Genentech Intern Day and present your learnings at an ECD forum

Qualification

Clinical researchGCPData AnalyticsAI toolsGoogle SuiteTime managementOrganizational skillsCommunication skillsCollaboration skills

Required

Must have attained a Bachelor's Degree (not currently enrolled in a graduate program)
Must be pursuing a Master's Degree (enrolled student)
Must have attained a Master's Degree
Must be pursuing a PhD (enrolled student)
Must have attained a PhD
Required Majors: Life sciences, Clinical sciences (e.g., PhD, PharmD, NP, PA, MPH) or a related scientific field, Risk Management, Biotechnology, Engineering (Biomedical), Data Analytics or Regulatory Science/Affairs

Preferred

Ability to work independently with minimal guidance
Excellent time management, strong organizational skills, and attention to detail
Ability to interact and collaborate effectively within a team setting and with both junior and senior level professionals
Proficient in utilizing AI tools (e.g., Gemini, ChatGPT, NotebookLM, Google Vids) and business software, including Google Suite, Word Excel, Powerpoint
Drug development experience, particularly in clinical research and GCP, is a plus
Excellent communication, collaboration, and interpersonal skills
Complements our culture and the standards that guide our daily behavior & decisions: Integrity, Courage, and Passion

Benefits

Paid holiday time off benefits

Company

Genentech

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Genentech is a biotechnology research company that specializes in genetic testing and personalized medicines.

H1B Sponsorship

Genentech has a track record of offering H1B sponsorships. Please note that this does not guarantee sponsorship for this specific role. Below presents additional info for your reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (167)
2024 (148)
2023 (150)
2022 (178)
2021 (121)
2020 (158)

Funding

Current Stage
Public Company
Total Funding
unknown
2009-03-26Acquired
1999-07-20IPO
1976-01-01Series Unknown

Leadership Team

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Ashley Magargee
Chief Executive Officer
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Michael Laird
Vice President, Global MSAT Drug Substance Biologics Technology and Commercial Products Support
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Company data provided by crunchbase