Clinical Project Manager II - Virology; Sponsor Dedicated - US Remote; Preference Hybrid Fo

Overview

Clinical Project Manager II - Virology (Sponsor Dedicated - US Remote; Preference for Hybrid Foster City, CA)

Syneos Health is a leading fully-integrated life sciences services organization built to accelerate customer success. We partner with innovators at every point across the drug development and commercialization continuum, helping them navigate complexity, anticipate change and accelerate progress. Our Clinical Solutions team members act with a drug development mindset, applying their years of experience and deep expertise to truly understand customer needs and represent those in the solutions we shape.

Whether you join us in a Functional Service Provider partnership or a Full-Service environment, you''ll collaborate with passionate problem solvers, innovating as a team to help our customers achieve their goals. We are agile and driven to deliver - for one another, our customers, and, most importantly, for those in need. Discover what your 25,000 future colleagues already know:

• We are passionate about developing our people, through career development and progression; supportive and engaged line management; technical and therapeutic area training; peer recognition and total rewards program.
• We are committed to building an inclusive culture - where you can authentically be yourself. Central to this is our purpose - Driven to Deliver - which captures the passion of our colleagues to show up each day and shape solutions that have the ability to dramatically impact someone''s life.
• We are continuously building the company we all want to work for and our customers want to work with. Why? Because we know that when we bring together smart colleagues from across the world, we can shape the future of healthcare, driving impact for customers and defining the pace of patient progress.

Clinical Project Manager II - Virology

Sponsor Dedicated | Remote (US)

(Preference for Hybrid Foster City, CA-Based Candidates)

Are you a Clinical Project Manager who can independently drive global Phase II-III clinical trials from start-up through closeout - while also staying deeply engaged in the operational details that keep studies running successfully day to day?

This is an opportunity to join a highly collaborative, fast-paced clinical operations team supporting innovative virology programs within a sponsor-dedicated environment. The team is specifically seeking a hands-on operational leader - someone who is comfortable rolling up their sleeves, navigating complex study execution challenges directly, and operating far beyond high-level oversight alone.

The ideal candidate is someone who genuinely enjoys being "in the weeds" operationally. You should be comfortable actively reviewing study documentation, managing operational trackers, troubleshooting systems and processes, partnering closely with CROs and regional leads, and driving execution across all facets of study operations.

This is not a purely strategic oversight role. The team is looking for someone who understands what strong operational execution looks like because they have personally done the work themselves.

While virology experience is strongly preferred, candidates with strong global Phase II-III clinical trial management experience in other therapeutic areas will also be considered.

This team values operational excellence, accountability, collaboration, urgency, adaptability, and proactive problem-solving. Leadership is highly supportive, mentorship-focused, and invested in helping strong performers expand their impact and career trajectory.

While remote/home-based candidates may be considered, priority will be given to candidates located in or near Foster City, California, with the ability to work onsite 2-3 days per week.

• Lead and manage global Phase II-III clinical trials from study start-up through database lock and closeout with minimal oversight
• Serve as the operational lead responsible for driving study execution, timelines, deliverables, risks, and overall trial performance
• Provide close oversight of CROs, regional leads, vendors, and study teams to ensure operational alignment, accountability, and execution quality
• Independently manage and support IRT/IXRS activities, including study setup oversight, ongoing maintenance, issue management, troubleshooting, and cross-functional coordination
• Maintain direct involvement in day-to-day study operations, including reviewing monitoring reports, study documentation, operational deliverables, and site-related activities
• Oversee site management and study maintenance activities to ensure studies remain inspection-ready and operationally compliant
• Review and manage informed consent forms (ICFs), study documentation, and operational materials to support quality and compliance expectations
• Manage operational trackers, including 1572 trackers and other critical study maintenance trackers, ensuring accuracy, completeness, and timely follow-up
• Drive study team meetings by…