Who We Are
Verily is a subsidiary of Alphabet that is using a data-driven approach to change the way people manage their health and the way healthcare is delivered. Launched from Google X in 2015, Our purpose is to bring the promise of precision health to everyone, every day. We are focused on generating and activating data from a variety of sources, including clinical, social, behavioral and the real world, to arrive at the best solutions for a person based on a comprehensive view of the evidence. Our unique expertise and capabilities in technology, data science and healthcare enable the entire healthcare ecosystem to drive better health outcomes.
Description
Together with researchers, clinicians, engineers, designers, advocates, and volunteers, we're collaborating to design the next generation of healthcare tools and services. Verily’s Clinical Studies Platform (CSP) business is focused on transforming evidence generation within clinical research. Our portfolio of solutions is focused on: 1) participant engagement to optimize and diversify participant recruitment and retention, 2) longitudinal registries and communities to support the continuous evaluation of medical products, 3) a software platform and services portfolio to support participant and data centric clinical trials, and 4) digital biomarkers for generating new types of data and insights.
As a Program Manager on Verily’s Study Operations team, you will lead cross functional teams in clinical study planning, execution, software deployment, and change management. You will oversee program management work streams for studies ensuring relevant practices (e.g. Good Clinical Practices, Good Pharmacoepidemiology Practices, Common Rule) and relevant Standard Operating Procedures (SOPs) are met as required. You will be responsible for maintaining and communicating timelines, tracking and monitoring risks, and translating business requirements to software requirements to ensure on time launch and successful execution.
Responsibilities
- Support program governance with internal and external stakeholders gathering and maintaining records and reports for KPIs, metrics, and milestones.
- Provide input for developing study-related materials, such as kick off materials, meeting agendas, minutes, decision logs, charters, and user acceptance testing plans.
- Identify and mitigate risks and apply strong problem-solving skills to ensure timely resolution of all project-related issues.
- Support the planning and setup, maintenance, and closeout phases of multiple concurrent clinical research studies. Develop and maintain project artifacts (timeline, project management plan, budget etc.) that support team communication, efficiency, and regulatory compliance.
- Independently execute on study objectives as a workstream(s) lead and/or study program lead.
Qualifications
Minimum Qualifications:
- BA/BS/BScN degree in health or biologic science, or equivalent practical experience.
- PMP.
- 8+ years of clinical study management experience in registries, observational research, RWD/E, or clinical trials as a clinical study lead/project manager.
- Experience in study project management and prior management of contracted resources/CROs.
Preferred Qualifications
- Master's degree in health or biologic science, or equivalent practical experience.
- Advanced knowledge of Good Pharmacoepidemiology Practices.
- Deep knowledge of the range of tools used in the clinical study management space and associated technology solutions.
The US base salary range for this full-time position is $104,000-$160,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.
Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits.
Why Join Us
Build What’s Vital.
At Verily, you are a part of something bigger. We are a diverse team of builders innovating at the intersection of health and technology—united by a shared spirit of curiosity, resilience and determination to make better health possible for all. This builder mindset means your fingerprints will be on the work that shapes the future of health. Fulfilling our precision health purpose starts with the health of our Veeps (what we call our employees), which is why we offer flexibility, resources, and competitive benefits to support you in your whole-person well being. We believe diversity of thought drives innovation—we unite the brightest minds, and encourage all Veeps to bring their lived experience to work with them.
If this sounds exciting to you, we would love to hear from you.
You can find out more about our company culture on our LinkedIn Company Page and Verily Careers page.
