Assistant Manager, Site-ICRA
Core
Supervise Clinical Site Operations (CSO) teams to support US, Canada, and LATAM clinical trials from start-up to closure, ensuring protocol compliance and audit readiness.
Role type
Senior IC clinical research operations manager
Builds
Clinical trial execution and site management processes
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
People management, clinical research operations, regulatory compliance, site activation/maintenance, audit preparation, staff hiring and training, process improvement
Preferred skills
SoCRA/ACRP certification, regulatory audit experience, clinical trial lifecycle expertise
Technologies
CTMS, Trial Master File systems, Microsoft Office Suite
Responsibilities
Supervise In-house Clinical Research Associates; ensure regulatory and protocol compliance; manage site lifecycle activities (invitation, activation, maintenance, closure); prepare for and support site audits; hire, train, and develop staff; lead process improvement projects.
Seniority
Manager, hands-on leadership