What are the responsibilities and job description for the Clinical Program Manager position at Verily?
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
The Clinical Program Manager will be an integral member of the growing Digital Biomarkers and Device Operations team, as Verily is seeking to improve the way clinical trials are conducted and evidence is generated using advanced software and sensor technology. In this role, you will oversee the planning and execution of clinical studies that are sponsored by Verily or an industry client, and include the deployment of one or more medical devices. You will interact closely with a variety of teams at Verily, as well as clients from industry. These studies will include overseeing external Clinical Sites or our internal Clinical Verily Site.
We are looking for an individual who is skilled in program managing a range of clinical study designs, including remote/decentralized/hybrid approaches, has excellent collaboration and communication skills, and is intellectually curious about new ideas for how to execute studies within the regulated research setting. Since Verily products include digital biomarkers, hardware sensors, software, and algorithm development, your experience in the medical devices space, and ability to manage different research programs will be an important aspect of the work. You have outstanding people skills and have demonstrated your ability to coach your team members or co-workers.
Together with researchers, clinicians, engineers, designers, advocates, and volunteers, we're collaborating to design the next generation of healthcare tools and services. As a Clinical Program Manager, you will work with teams across Verily to drive clinical study planning, execution, and closeout to meet the needs of our external clients and clinical trial participants.
Responsibilities
- As a Clinical Program Manager, you will be responsible for coordinating cross-functional team members, external stakeholders, and activities across all geographies, liaising with project leadership to ensure that deliverables (timeline, quality, productivity) are met.
- You will oversee all operational aspects for the implementation of clinical trial activities from study start-up through database lock, ensuring Good Clinical Practices (GCPs) and relevant Standard Operating Procedures (SOPs) are met.
- Your role will implement cross-functional risk evaluation, mitigation, and management strategies aligned with Verily and client risk management frameworks. You will seek to improve the operational delivery of clinical studies by closely aligning and developing processes with multidisciplinary stakeholders (product, UX, legal, quality, regulatory, etc.).
- Communicate directly with external clients/sponsors to drive operational work design and provide updates on timelines; build and track patient recruitment and progress to study timelines.
Qualifications
- BS/BSN degree in health or biologic science, or equivalent practical experience.
- At least 3 years of clinical research experience in the medical device, biopharmaceutical or diagnostics industry, including 2 years of experience as a clinical study lead/project manager.
- Experience in study project management and prior management of contracted resources/CROs is required.
- Exceptional organizational, documentation and general program management skills in a clinical trial setting, including stakeholder management with medical personnel and scientific. research colleagues; excellent communication skills, with experience communication to executives. Working knowledge of Good Clinical Practices and current knowledge of FDA regulations for clinical trials.
- Master's degree in health or biologic science, or equivalent practical experience.
- PMP certification.
- Strong working knowledge of project management tools such as spreadsheets, Google docs, and project tracking software.
- Strong interpersonal skills with sensitivity to changing personalities and priorities.
- Ability to improvise, work efficiently and respond quickly to changes and a dynamic work-flow; proven ability to manage complex projects involving multiple stakeholders, and in a fast pace environment
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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, which is why we offer flexibility, resources, and competitive benefits to support you in your whole-person well being.
Our culture reflects the behaviors that stem from living our values every day in how we Innovate Healthcare and Technology, Gain Velocity as One Verily, and Respect Individuals. As One Verily, we uphold our collective accountability to sustain this culture and to create a VIBE (Verily’s Culture of Inclusion, Belonging, and Equitability) where all Veeps feel included, a sense of belonging, and have opportunities to grow.
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.
Salary : $104,000 - $160,000
