Site Management Associate I
HybridNo visa sponsorship
Core
Administrative and operational support for clinical research sites, managing documentation, supplies, audits, and communication between sites and vendors.
Role type
Site Management Associate
Builds
Study documentation, supply chains, audit readiness, and site-vendor communication flows
Domain
Clinical Research / Medical Science
Deliverable
dashboards & analysis
Required skills
Clinical research industry knowledge, site/vendor communication, regulatory/ethics committee submissions, audit coordination, EDC completion tracking, CTMS management, training coordination, document management (TMF/ISF), safety information flow, MS Office proficiency (Word, Excel, Outlook, PowerPoint), English typing (40 wpm)
Preferred skills
None stated
Technologies
CTMS, EDC systems, TMF, ISF, MS Office suite
