Study Management Associate III /Clinical Trial Manager
Core
Lead and execute global Phase 0-4 clinical trials independently, ensuring quality, efficiency, and compliance with timelines and budget.
Role type
Senior IC Clinical Trial Manager (Study Management Associate III)
Builds
Global clinical trial operations from inception to closure
Domain
Biopharmaceuticals / Clinical Research
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Vendor management, global recruitment strategy, risk identification and mitigation, study material development, regulatory compliance (ICH/GCP), system management (EDC, IRT, CTMS, eTMF), stakeholder engagement, inspection readiness
Preferred skills
End-to-end study initiation to completion experience, global study exposure
Technologies
EDC, IRT, CTMS, eTMF, ePRO
Responsibilities
Lead cross-functional teams for global trial execution; manage external vendors and recruitment strategies; develop and maintain study protocols and materials; ensure inspection readiness; support global submission strategies; mentor team members
Seniority
Senior, hands-on IC
