Site Management Associate I
Core
Provide non-monitoring site management and administrative support for clinical research projects in Türkiye, serving as the main contact for investigative sites, vendors, and project teams.
Role type
Site Management Associate (Clinical Research)
Builds
Clinical trial operations and site coordination in Türkiye
Domain
Clinical Research / CRO
Deliverable
client delivery
Required skills
Trial record maintenance, regulatory document preparation, site payment coordination, EDC tracking, audit support, vendor communication, translation coordination, CTMS tracking
Preferred skills
Prior Site Coordinator experience, international CRO environment experience
Technologies
CTMS, EDC, MS Office, TMF, ISF
Responsibilities
Exchange data and documents between sites, vendors, and project teams; prepare regulatory and ethics committee submission documents; coordinate site payments and trial supplies; support query resolution and EDC completion; coordinate preparation for site audits and inspections; maintain Trial Master File (TMF) and Investigator Site Files (ISF); coordinate trial-related training for investigator sites.
Seniority
Entry-level / Associate
