Site Management Associate I
Core
Key support to clinical research projects, streamlining communication, maintaining systems, and managing documents & information.
Role type
Site Management Associate I
Builds
Clinical research operations and documentation
Domain
Clinical research / Life Sciences
Deliverable
dashboards & analysis
Required skills
Data exchange, supply chain management, regulatory submissions, audit coordination, document management, safety information flow
Preferred skills
MS Office proficiency, English proficiency, organizational skills, problem-solving, multitasking, customer service
Technologies
Trial Master File (TMF), Investigator Site Files (ISF), corporate tracking systems
Responsibilities
Exchanges data and documents between sites, vendors, and project teams; manages clinical supplies inventory and reconciliation; administers site and vendor payments; handles regulatory and ethics committee submissions; coordinates audit and inspection preparations; maintains TMF and ISF; ensures safety information flow.
Seniority
Entry-level
