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Syneos Health

Clinical Project Manager II – Virology, Phase I

Syneos Health

Clinical Project Manager II managing global Phase I virology clinical trials at Syneos Health. Overseeing operational execution and collaboration with cross-functional teams across the trial lifecycle.

Posted 7/9/2026full-timeRemote • Arizona, California, Maine, Ohio, Rhode Island • 🇺🇸 United StatesMid-LevelSenior💰 $95,000 - $175,700 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in managing global Phase I virology clinical trials, ensuring compliance with GCP and regulatory requirements while fostering collaboration among cross-functional teams. Proven ability to drive study execution, mitigate risks, and enhance operational performance through effective project management and communication skills.

Highest-signal resume keywords
Clinical Project ManagementPhase I Clinical TrialsGCP ComplianceRisk Identification and MitigationCross-Functional Team Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Trial Lifecycle ManagementStudy Documentation OversightOperational Performance MetricsBudget ManagementVendor Oversight
Soft Skills
Meeting FacilitationOrganizational LeadershipEmotional IntelligenceProblem SolvingCollaboration
Industry Keywords
CRO ManagementRegulatory RequirementsClinical OperationsBiometricsStudy Start-Up

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • 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

What you’ll need
  • 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

Comp & perks
  • 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