Site Management Associate II
No visa sponsorship
Core
Administrative support and coordination for clinical trial sites, managing documentation, communications, and regulatory submissions.
Role type
Administrative Site Management Associate
Builds
Clinical trial site files, regulatory submissions, and audit-ready documentation
Domain
Clinical Research / Pharmaceutical
Deliverable
dashboards & analysis
Required skills
Regulatory document preparation, site communication, audit coordination, EDC progress tracking, TMF management, ISF maintenance, training coordination, payment coordination, query resolution
Preferred skills
Vendor management, investigator meeting organization, internal coaching
Technologies
MS Word, MS Excel, MS Outlook, MS PowerPoint, vendor-related systems, EDC systems