Program Manager II, Clinical Research Operations, Platforms and Devices

Program Manager II, Clinical Research Operations, Platforms and Devices

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corporate_fareGoogleplaceSan Jose, CA, USA

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Mid

Experience driving progress, solving problems, and mentoring more junior team members; deeper expertise and applied knowledge within relevant area.

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Minimum qualifications:

• Bachelors degree or equivalent practical experience.

• 2 years of experience in program or project management.

• Experience integrating generative AI tools or Large Language Model (LLM) interfaces into workflows.

• Experience as a clinical research associate in sponsor-initiated clinical research operations.

Preferred qualifications:

• 2 years of experience managing cross-functional or cross-team projects.

• Experience in user experience research and ophthalmic optics, including a strong understanding of ophthalmic terminology, lens measurements, prescription interpretation, and optical measurements and equipment.

• Experience in consumer electronics, or wearables technologies.

• Familiarity with hardware development cycles and processes.

About the job

A problem isn't truly solved until it's solved for all. That's why Googlers build products that help create opportunities for everyone, whether down the street or across the globe. As a Program Manager at Google, you'll lead complex, multi-disciplinary projects from start to finish - working with stakeholders to plan requirements, manage project schedules, identify risks, and communicate clearly with cross-functional partners across the company. Your projects will often span offices, time zones, and hemispheres. Its your job to coordinate the players and keep them up to date on progress and deadlines.

As a Clinical Program Manager at Google, you will work with stakeholders to deliver on clinical outcomes and manage device use in alignment with clinical compliance requirements. You will plan study requirements with internal engineering teams and usher user evaluations through the entire product lifecycle. This includes managing Institutional Review Board (IRB) compliance, coordinating laboratory workflows, and communicating with project stakeholders.

You will be responsible for driving the day-to-day operations and logistics of clinical studies, serving as the primary liaison between study sites, managers, and regulatory bodies. Key duties include managing IRB submissions, maintaining the Trial Master File (TMF) to ensure GCP compliance, and coordinating the distribution of investigational devices and study supplies. Additionally, this role oversees subject enrollment tracking, monitors Case Report Form (CRF) data quality, and ensure all participant data, informed consent forms (ICFs), and Adverse Event (AE) reporting are accurate, legible, and fully compliant with ALCOA+ source documentation principles inside the Trial Master File (TMF).

The Platforms and Devices team encompasses Googles various computing software platforms across environments (desktop, mobile, applications), as well as our first party devices and services that combine the best of Google AI, software, and hardware. Teams across this area research, design, and develop new technologies to make our users interaction with computing faster and more seamless, building innovative experiences for our users around the world.

Individual pay is determined by factors including job-related skills, experience, and relevant education or training.

US: $132000 - $189000 (USD) + 15% bonus target + equity + benefits

Learn more about benefits at Google.

Responsibilities

• Manage day-to-day ophthalmic Rx program and device logistics and Collaborate with cross-functional partners including Clinical, Research Scientists, UX Researchers, Hardware/Software Engineering, and Regulatory to track program and study requirements, maintain schedules, and monitor study-readiness and compliance criteria.
• Manage study workflows by coordinating human subject test execution, managing evaluation logistics, and supervising clinical participant and laboratory logistics alongside research scientists and program stakeholders.
• Identify risks, blockers, and changing timelines early (such as recruitment bottlenecks, site enrollment delays, or regulatory hurdles), working alongside Program and Clinical Leads to triage operational issues.
• Contribute to team operational excellence by supporting clear clinical program tracking mechanism.
• Manage administrative and operational program overhead, including compiling resource demands, drafting program-related status reports.

Information collected and processed as part of your Google Careers profile, and any job applications you choose to submit is subject to Googles Applicant and Candidate Privacy Policy.

Google is proud to be an equal opportunity and affirmative action employer. We are committed to building a workforce that is representative of the users we serve, creating a culture of belonging, and providing an equal employment opportunity regardless of race, creed, color, religion, gender, sexual orientation, gender identity/expression, national origin, disability, age, genetic information, veteran status, marital status, pregnancy or related condition (including breastfeeding), expecting or parents-to-be, criminal histories consistent with legal requirements, or any other basis protected by law. See also Googles EEO Policy, Know your rights: workplace discrimination is illegal, Belonging at Google, and How we hire.

If you have a need that requires accommodation, please let us know by completing our Accommodations for Applicants form.

Google is a global company and, in order to facilitate efficient collaboration and communication globally, English proficiency is a requirement for all roles unless stated otherwise in the job posting.

To all recruitment agencies: Google does not accept agency resumes. Please do not forward resumes to our jobs alias, Google employees, or any other organization location. Google is not responsible for any fees related to unsolicited resumes.

Equity is granted exclusively and discretionarily by Alphabet Inc. on the basis of an agreement concluded between you and Alphabet Inc. Alphabet Inc. is your sole contractual partner with respect to equity grants. GSU grants are not guaranteed, are discretionary, are subject to approval by the Alphabet Inc. board of directors or its delegate, the terms of the relevant Alphabet Inc. stock plan, and your grant agreement. They have no impact on statutory payments. Current or past grants do not confer an acquired right.