Clinical Project Manager II

• Early Phase Virology /Healthy Volunteer Studies (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: Why Syneos Health
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• 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. Job Responsibilities Clinical Project Manager II
• Early Phase Virology (Healthy Volunteer Studies)Sponsor Dedicated | Remote (US)Preference for Hybrid Foster City, CA-Based Candidates Are you a Clinical Project Manager with recent, hands-on experience leading the operational execution of Early Phase Healthy Volunteer clinical trials from protocol development through Clinical Study Report (CSR)?

Do you thrive in a lean environment where you are expected to independently drive study delivery, collaborate across functions, and maintain direct ownership of day-to-day study execution? This opportunity supports innovative early-phase virology programs within a sponsor-dedicated environment. The team is seeking an experienced Clinical Project Manager who brings deep operational expertise in Healthy Volunteer studies and can confidently lead complex Phase I clinical trials from start-up through closeout. Success in this role requires a highly organized, proactive individual who combines strong project leadership with hands-on operational execution. The ideal candidate has direct experience managing the day-to-day delivery of Early Phase Healthy Volunteer studies and can quickly contribute with minimal ramp-up. This position is best suited for someone who has maintained operational ownership of studies throughout the clinical trial lifecycle and has extensive experience working directly with sites, vendors, and cross-functional stakeholders to drive study execution. While remote candidates throughout the U.S. will be considered, preference will be given to candidates located in or near Foster City, California, with the ability to work onsite 2-3 days per week.

THE ROLE

As a Clinical Project Manager II

• Early Phase Virology, you will lead the operational execution of global Early Phase Healthy Volunteer studies while serving as the primary driver of study delivery across the clinical trial lifecycle.

You will oversee timelines, budgets, operational risks, study start-up activities, vendor performance, and cross-functional collaboration while ensuring studies are conducted in accordance with sponsor expectations and applicable quality requirements. This role requires an individual who can independently navigate the complexities of early-phase clinical development, work effectively within a lean team structure, and maintain direct involvement in study operations from protocol development through CSR completion.

WHAT YOU WILL DO

Lead and manage Early Phase Healthy Volunteer clinical trials from study start-up through closeout with minimal supervision. Drive day-to-day operational execution, study timelines, deliverables, and overall study performance. Serve as the primary operational point of contact for study sites. Lead operational activities across the full study lifecycle, including protocol development, study start-up, study conduct, database lock, and CSR completion. Oversee dose-escalation activities and support safety review processes required for Healthy Volunteer studies. Lead cross-functional collaboration with Clinical Pharmacology, Biomarkers, Biostatistics, Statistical Programming, Medical Monitoring, Data Management, and other key stakeholders. Manage vendor relationships and monitor operational performance to support successful study execution. Facilitate study team meetings, document key decisions, and drive accountability for action items. Identify operational risks, develop mitigation strategies, and proactively resolve issues impacting study delivery. Maintain oversight of study documentation, trial metrics, and operational deliverables. Ensure studies are conducted in compliance with GCP, SOPs, regulatory requirements, and sponsor expectations. Contribute to process improvements and operational best practices that enhance study execution.

WHO YOU ARERequired Qualifications Significant Clinical Project Management experience with responsibility for independently managing clinical trials across the full study... For full info follow application link.