Senior Associate Director, Global Site Management

Kps-Life; Cambridge (MA); Hybrid; USD 150,000 - 210,000; Full time

Job summary

KPS Life seeks an Associate Director, Global Site Management to lead RBQM-driven site monitoring across a global trial portfolio. The role involves managing CRO/FSP partners, supervising a team of monitors, and driving inspection readiness and process improvements.

The candidate will collaborate with trial management, QA, and vendor teams to ensure compliant, efficient study delivery in a fast-paced environment. Travel up to 25% may be required.

Qualifications

• Extensive experience leading monitoring teams in clinical trials.
• Deep RBQM knowledge and risk-based quality management.
• Strong communication and collaboration with cross-functional teams.

Responsibilities

• Directs study- and program-level monitoring strategy across portfolios.
• Oversees CRO/FSP partners, CRA resources, and site management activities.
• Ensures inspection readiness and regulatory compliance (ICH/GCP).
• Leads process improvements and innovative monitoring approaches.
• Manages budgets, staffing, and performance metrics for teams.

Skills

RBQM expertise

FSP/CRO oversight

Team leadership

Quality monitoring

Risk-based thinking

ICH/GCP knowledge

Education

Bachelor's degree

Job description

KPS Life seeks an Associate Director, Global Site Management to lead RBQM-driven site monitoring across a global trial portfolio. The role involves managing CRO/FSP partners, supervising a team of monitors, and driving inspection readiness and process improvements.

The candidate will collaborate with trial management, QA, and vendor teams to ensure compliant, efficient study delivery in a fast-paced environment. Travel up to 25% may be required.