Clinical Project Manager II — Hybrid, Impactful Trials

United Therapeutics Corporation; Durham, Northern (NC, KY); Hybrid; USD 110,000 - 140,000; Full time

Benefits offered by this job

Hybrid in-office schedule

Travel up to 30%

Job summary

United Therapeutics Corporation seeks a Clinical Project Manager II/Senior Clinical Project Manager to drive local or regional clinical trials from start-up to close-out. You will oversee budgets, timelines, and cross-functional collaboration with vendors and study teams in a fast-paced environment.

The role requires a strong clinical research background, familiarity with EDC/CTMS, and leadership to manage high-workload periods while maintaining study quality and compliance.

Qualifications

• Bachelor’s degree in related field required; 8+ years in clinical study management or project management.
• Master’s degree preferred; 6+ years in clinical study management or project management.

Responsibilities

• Lead local/regional clinical trials from start-up to close-out.
• Oversee study budgets and timelines, ensure quality and performance metrics.
• Coordinate with cross-functional teams, vendors, and management.
• Escalate timelines or performance concerns promptly to line management.
• Ensure SOPs, ICH/GCP guidelines, and local regulations are followed.
• Prepare interim and primary analysis reports and support Investigator Meetings.

Skills

Project management

Communication skills

GCP/ICH knowledge

MS Office proficiency

Team leadership

Education

Bachelor’s degree in related field

Master’s degree in related field

Tools

EDC

CTMS

Job description

United Therapeutics Corporation seeks a Clinical Project Manager II/Senior Clinical Project Manager to drive local or regional clinical trials from start-up to close-out. You will oversee budgets, timelines, and cross-functional collaboration with vendors and study teams in a fast-paced environment.

The role requires a strong clinical research background, familiarity with EDC/CTMS, and leadership to manage high-workload periods while maintaining study quality and compliance.