Global Clinical Trial Lead (Phase I–IV)

CTI; Covington (KY); Hybrid; USD 110,000 - 160,000; Full time

Benefits offered by this job

Hybrid work opportunities

Health benefits

Vacation packages

Paid parental leave

Job summary

CTI Clinical Trial and Consulting Services is seeking a Senior Clinical Project Manager to lead and oversee multi‑phase clinical trials, ensuring time, cost, and quality goals are met. The role involves global coordination across regions, strategic planning, and client communication, with a focus on trial timelines, budgets, and regulatory compliance.

Ideal candidates will have 6+ years in clinical research within CROs or pharma settings, a relevant bachelor’s degree (graduate degree preferred),

Qualifications

• Bachelor’s degree in allied health fields with clinical trial management experience or equivalent.
• Graduate degree preferred for advanced roles.
• Strong project management skills in a CRO, hospital, or pharma setting.

Responsibilities

• Oversee planning, execution, and close-out of trials (Phase I–IV) as global trial lead.
• Coordinate across teams and regions to ensure ICH-GCP compliance and regulatory adherence.
• Develop trial timelines, deliverables, budgets, and resources for timely execution.
• Lead study meetings and prepare status reports for client oversight and documentation.
• Monitor timelines, KPIs, scope, budget, and vendor deliverables; escalate risks as needed.
• Identify and mitigate trial risks and communicate action plans to meet milestones.
• Ensure TMF completeness and site performance for inspection readiness.

Skills

Clinical trial management

Project management

Regulatory knowledge

Communication

Risk management

Education

Bachelor’s degree in allied health fields

Graduate degree preferred

Job description

CTI Clinical Trial and Consulting Services is seeking a Senior Clinical Project Manager to lead and oversee multi‑phase clinical trials, ensuring time, cost, and quality goals are met. The role involves global coordination across regions, strategic planning, and client communication, with a focus on trial timelines, budgets, and regulatory compliance.

Ideal candidates will have 6+ years in clinical research within CROs or pharma settings, a relevant bachelor’s degree (graduate degree preferred),