Assistant Manager, Site-ICRA
Core
Supervise a team of In-house Clinical Research Associates to support US, Canada, and LATAM clinical trial operations including site activation, maintenance, compliance, and closure.
Role type
Senior management IC (Assistant Manager, Clinical Site Operations)
Builds
Clinical trial execution and site management for Abbott's global healthcare portfolio
Domain
Healthcare / Clinical Research
Required skills
People management, clinical research knowledge, regulatory compliance, site audit readiness, process improvement, team development, project planning
Preferred skills
SoCRA or ACRP certification, regulatory audit experience, clinical trial lifecycle expertise
Technologies
Microsoft Office Suite, CTMS, Trial Master File systems
Responsibilities
Supervise and develop a team of Clinical Research Associates; ensure regulatory and protocol compliance for assigned clinical studies; manage site activation, maintenance, and closure activities; lead process improvement projects; partner with Site and Project Management to achieve study goals.
Seniority
Senior, hands-on IC with people management
