Site Management Associate I
Core
Support clinical research projects by managing site communications, clinical supplies, regulatory submissions, and document management.
Role type
Site Management Associate
Builds
Clinical research operations and documentation
Domain
Clinical research / Life sciences
Deliverable
dashboards & analysis
Required skills
Data exchange, inventory management, payment administration, regulatory submissions, audit coordination, TMF maintenance, ISF management, safety information flow
Preferred skills
MS Office proficiency, organizational skills, problem-solving, multi-tasking
Technologies
Trial Master File (TMF), Investigator Site Files (ISF), corporate tracking systems
Responsibilities
Exchange data and documents between sites, vendors, and project teams; manage clinical supplies inventory and distribution; administer site and vendor payments; handle regulatory and ethics committee submissions; coordinate audit preparations; maintain TMF and ISF; ensure safety information flow.
Seniority
Entry-level