Clinical Project Manager II – Virology, Phase I

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🌵 Arizona, California, +3 more states – Remote

🌵 Arizona – Remote 🏄 California – Remote 🦞 Maine – Remote 🏈 Ohio – Remote ⚓ Rhode Island – Remote

💵 $95k - $175.7k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

🏥 Clinical Operations

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Syneos Health

WebsiteLinkedInAll Job Openings

10,000+ employees

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

Syneos Health is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. They translate unique clinical, medical affairs, and commercial insights into outcomes to address modern market realities. By utilizing advanced technologies and insights, Syneos Health collaborates with clients to speed the delivery of important therapies to patients worldwide, offering services that span the entire clinical-to-commercial spectrum.

📋 Description

• 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

🎯 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