Clinical Project Manager II – Virology /Phase I (Sponsor Dedicated - US Remote; Preference for [...]

Clinical Project Manager II – Virology (Phase I)

Position: Sponsor‑Dedicated, Remote (US) Preference for Hybrid Foster City, CA‑Based Candidates Company: Syneos Health

We are looking for an experienced Clinical Project Manager to independently lead global Phase I virology trials from study start‑up through closeout.

The role requires operational leadership, cross‑functional collaboration, and proactive risk management to deliver high‑quality early‑phase studies.

Key Responsibilities

• Lead and manage global Phase I virology clinical trials from study start‑up through closeout.
• Drive overall study execution, timelines, deliverables, risks, budgets, and operational performance.
• Provide oversight and accountability for CROs, vendors, and cross‑functional partners to ensure high‑quality study execution.
• Build strong collaborative relationships with Clinical Operations, Data Management, Regulatory, Medical, Clinical Supply, Biometrics, and other stakeholders.
• Lead study team meetings by establishing clear agendas, facilitating productive discussions, documenting key decisions, and ensuring timely completion of action items.
• Proactively identify operational risks, develop mitigation strategies, and drive issue resolution before timelines or quality are impacted.
• Guide study teams through key transitions across the clinical trial lifecycle while ensuring seamless operational execution.
• Maintain oversight of study documentation, trial metrics, operational deliverables, and inspection readiness activities.
• Ensure compliance with GCP, SOPs, regulatory requirements, and sponsor expectations.
• Foster accountability across study teams while creating an environment of collaboration, transparency, and shared ownership.
• Contribute to process improvements and operational best practices that enhance study execution and team performance.
• Required Qualifications
• Bachelor’s degree in a scientific or healthcare‑related field (or equivalent combination of education and experience).
• Significant Clinical Project Management experience with responsibility for independently managing clinical trials across the full study lifecycle (5+ years).
• Demonstrated experience leading Phase I and/or other early‑phase clinical studies.
• Strong understanding of the complete clinical trial lifecycle, with the ability to independently manage study transitions from start‑up through closeout.
• Proven experience overseeing CROs, vendors, and external partners within global clinical trials.
• Excellent project management, organizational, and operational leadership skills.
• Strong meeting facilitation skills with the ability to lead productive discussions, build alignment, and ensure accountability for follow‑up actions.
• Exceptional verbal and written communication skills with demonstrated emotional intelligence and professionalism when working across diverse stakeholder groups.
• Ability to lead cross‑functional teams while effectively balancing multiple priorities in a fast‑paced environment.
• Demonstrated ability to proactively identify risks, solve problems independently, and drive successful study execution with minimal direction.
• Preferred Qualifications
• Virology clinical trial experience strongly preferred.
• Experience managing global Phase I clinical trials within pharmaceutical, biotechnology, or CRO environments.
• Stable career progression demonstrating increasing responsibility and leadership in clinical project management.
• Experience working within sponsor‑dedicated or embedded sponsor models.
• Experience managing multiple vendors and complex cross‑functional partnerships.
• Demonstrated success working in highly collaborative, fast‑paced, execution‑focused environments.

Benefits

Potential benefits include a company car or car allowance, health benefits (Medical, Dental, Vision), 401(k) company match, Employee Stock Purchase Plan, performance‑based commissions/bonuses, and flexible paid time off (PTO) and sick time.

Eligibility for paid sick time may vary by state or municipality.

• Salary Range
• $95,000.00 – $175,700.00

EEO Statement

Syneos Health is an equal opportunity employer.

We comply with all applicable federal, state, and municipal paid sick time requirements.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.

Additional Information

Tasks, duties, and responsibilities as listed in this job description are not exhaustive.

The Company reserves the right to assign additional duties and responsibilities.

The Company will determine what constitutes equivalent qualifications.

The Company is committed to compliance with the Americans with Disabilities Act and will provide reasonable accommodations when appropriate.

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