Site Management Associate
Core
Support clinical trial sites through start-up, conduct, and closeout activities to ensure compliance with protocols and regulations.
Role type
Site Management Associate
Builds
Clinical trial site activations and study execution
Domain
Clinical research / Healthcare
Required skills
Regulatory compliance, site startup management, contract coordination, document preparation, IRB/ethics committee liaison, site readiness verification, supply setup, troubleshooting
Preferred skills
Health or science degree, clinical research experience, Microsoft Office proficiency, clinical systems knowledge (EDC, CTMS, eTMF)
Technologies
EDC, CTMS, eTMF, Microsoft Office
Responsibilities
Develop site initiation timelines, prepare startup documentation (contracts, consents), coordinate with contracts/budget teams, submit regulatory documents, verify site readiness, participate in kick-off meetings, troubleshoot activation issues, setup study supplies.
Seniority
Mid-level, hands-on IC
