Global Clinical Project Director — Hybrid Trials

SystImmune; Princeton (NJ); Hybrid; USD 220,000 - 280,000; Full time

Benefits offered by this job

Premium health coverage

STD/LTD benefits

401(k) with company match

Vesting after 5 years

15 days PTO

Sick leave

11 paid holidays

Job summary

SystImmune is seeking a Senior Global Director, Clinical Project Management to oversee global clinical trials from initiation to completion. The role ensures regulatory compliance, manages timelines and budgets, and fosters collaboration among investigators, vendors, and cross-functional teams.

The position emphasizes leadership of regional CPMs, CRAs, and CTAs, while maintaining high-quality data and trial integrity. Based in Princeton, NJ with hybrid work expectations and ~25% travel.

Qualifications

• Bachelor’s degree in Life Sciences, Nursing, or a related field.
• Minimum of 15 years of experience in Clinical Trial Management with demonstrated people leadership.
• Strong experience with early-phase studies; late-phase experience is a plus.
• Solid understanding of GCP and regulatory requirements.
• Excellent organizational, project management, and cross-functional leadership skills.
• Effective communication and collaboration in a team environment.

Responsibilities

• Oversee the planning and execution of global clinical trials from initiation to completion.
• Develop and implement study protocols, timelines, and budgets.
• Manage site selection, initiation, monitoring, and closeout activities.
• Ensure compliance with GCP and regulatory guidelines across trials.
• Coordinate with investigators, vendors, and regulatory bodies to drive study success.
• Monitor data collection for accuracy and integrity; manage risk and issues.

Job description

SystImmune is seeking a Senior Global Director, Clinical Project Management to oversee global clinical trials from initiation to completion. The role ensures regulatory compliance, manages timelines and budgets, and fosters collaboration among investigators, vendors, and cross-functional teams.

The position emphasizes leadership of regional CPMs, CRAs, and CTAs, while maintaining high-quality data and trial integrity. Based in Princeton, NJ with hybrid work expectations and ~25% travel.