Global Clinical Trial Manager

Syneos Health/ inVentiv Health Commercial LLC

Alaska

On-site

USD 90,000 - 130,000

Full time

14 days+

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Benefits offered by this job

Company car or car allowance
Health benefits
401k match

Job summary

Syneos Health is seeking a Clinical Trial Manager for Full Service operations. You will oversee site management, monitoring, data integrity, and ensure regulatory compliance while coordinating with CRAs, CeMs, and data management teams.

You will lead risk assessments, manage budgets, and drive study milestones in a global environment, with travel up to 20% as needed. Strong collaboration and leadership are essential.

Qualifications

  • Bachelor's degree or RN in a related field or equivalent.
  • Demonstrated ability to lead and align teams to achieve milestones.
  • Experience in international environments and trial management.
  • Knowledge of GCP/ICH guidelines and regulatory requirements.
  • Moderate travel ~20%.

Responsibilities

  • Oversee site management, clinical monitoring and central monitoring with patient safety and data integrity focus.
  • Review study scope, budget and protocol to align the clinical team with obligations and parameters.
  • Identify risks to deliverables and escalate to project management as needed.
  • Develop and present risk mitigations; participate in key meetings.
  • Coordinate with functional leaders to meet milestones and plans (SOPs, CMP, data plans).
  • Maintain study tools/templates and ensure CTMS and dashboards are available.
  • Provide training to study team on protocol specifics, CRF, dashboards and timelines.
  • Oversee resource allocations for CRAs/Central Monitors and track progress.

Skills

Clinical trial management
Risk-based monitoring
Regulatory compliance
Cross-functional collaboration
Budget management

Education

Bachelor's degree or RN in related field

Job description

Syneos Health is seeking a Clinical Trial Manager for Full Service operations. You will oversee site management, monitoring, data integrity, and ensure regulatory compliance while coordinating with CRAs, CeMs, and data management teams.

You will lead risk assessments, manage budgets, and drive study milestones in a global environment, with travel up to 20% as needed. Strong collaboration and leadership are essential.

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