Site Management Associate I
Core
Support clinical research projects by managing site communications, documents, and regulatory compliance.
Role type
Site Management Associate I (Clinical Research)
Builds
Clinical trial operations at investigative sites
Domain
Clinical Research / Life Sciences
Deliverable
client delivery
Required skills
Document management, regulatory compliance, site audit coordination, clinical supply chain management, CTMS data tracking, vendor coordination, pre-study facility testing, safety information flow management
Preferred skills
CTA experience, international administrative experience, local regulations knowledge
Technologies
CTMS, EDC, TMF, ISF, MS Office
Responsibilities
Serve as main contact between site personnel and CRA for query resolution; Manage TMF and ISF documentation; Coordinate site audits and inspections; Ensure clinical supply order and inventory management; Track site event information in CTMS; Arrange site training; Ensure regulatory and ethics committee submissions.
Seniority
Individual Contributor, Entry to Mid-level