Global Site Management Lead - Associate Director

kps life; New Jersey; Hybrid; USD 180,000 - 240,000; Full time

Job summary

KPS Life is seeking an Associate Director, Global Site Management to lead RBQM-driven site monitoring strategies across a sponsor portfolio. The role requires building strong, senior-level relationships with CROs, FSPs, and study teams while guiding global site operations.

Located on site 3 days per week in Armonk, NY, Warren, NJ or Cambridge, MA, you will drive strategy, ensure inspection readiness, and mentor a team of monitoring professionals to deliver high-quality data and compliant trial

Qualifications

• 10+ years of clinical trial experience in RBQM and supplier oversight.
• Proven success managing CRAs and supervisors.
• Strong strategic leadership and cross-functional collaboration.
• Experience with ICH GCP and regulatory standards.
• Able to design and oversee monitoring strategies for studies and programs.

Responsibilities

• Directs the study and program-level monitoring strategy across a portfolio of studies.
• Manages budgets for teams, large projects, or multiple related projects.
• Oversees CRO partners and FSP/CRA performance, escalation, and issue resolution.
• Leads inspection readiness activities and regulatory GCP inspections/audits.
• Establishes productive investigator site relationships and cross-functional communications.

Skills

Team management

RBQM knowledge

RBM knowledge

CRO/FSP oversight

Clinical trial ops

Vendor management

Strategic leadership

Communication

Cross-functional collaboration

Education

Bachelor’s Degree

Job description

KPS Life is seeking an Associate Director, Global Site Management to lead RBQM-driven site monitoring strategies across a sponsor portfolio. The role requires building strong, senior-level relationships with CROs, FSPs, and study teams while guiding global site operations.

Located on site 3 days per week in Armonk, NY, Warren, NJ or Cambridge, MA, you will drive strategy, ensure inspection readiness, and mentor a team of monitoring professionals to deliver high-quality data and compliant trial