Site Management Associate I
Core
Key support to clinical research projects, streamlining communication, maintaining systems, and managing documents and information for investigative sites and vendors.
Role type
Site Management Associate I
Builds
Clinical research operations and documentation for medical science projects
Domain
Clinical research / Life sciences
Deliverable
client delivery
Required skills
Data exchange, clinical supply inventory management, regulatory submission coordination, audit preparation, TMF maintenance, ISF management, safety information flow
Preferred skills
Translation status checking, meeting organization
Technologies
MS Office, Trial Master File (TMF), Investigator Site Files (ISF)
Responsibilities
Exchange data and documents between sites, vendors, and project teams; manage clinical supplies inventory and reconciliation; administer site and vendor payments; handle regulatory and ethics committee submissions; coordinate audit and inspection preparations; maintain TMF and ISF; ensure safety information flow
Seniority
Entry-level, hands-on support
