Clinical Project Manager II – Virology, Phase I
Location
Arizona + 4 moreAll locations: Arizona | California | Maine | Ohio | Rhode Island
Posted
3 days ago
Salary
$95K - $175.7K / year
Seniority
Senior
Job Description
Clinical Project Manager II – Virology, Phase I
Syneos Health
• Lead and manage global Phase I virology clinical trials from study start-up through closeout with minimal supervision • 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
Job Requirements
- Bachelor's degree in a scientific or healthcare-related field (or equivalent combination of education and experience)
- 5+ years of Clinical Project Management experience with responsibility for independently managing clinical trials across the full study lifecycle
- 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.
Benefits
- Health benefits to include Medical, Dental and Vision
- Company match 401k
- Eligibility to participate in Employee Stock Purchase Plan
- Eligibility to earn commissions/bonus based on company and individual performance
- Flexible paid time off (PTO) and sick time
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