Senior Clinical Trial Associate
Core
Supports the planning, execution, and closeout of clinical studies in a regulated environment, ensuring compliance with protocols and GCP.
Role type
Senior Clinical Trial Associate
Builds
Clinical study programs and operational support for R&D
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Clinical trial operations, GCP principles, FDA regulations, Medical terminology, Study documentation management, Site coordination, Financial tracking, Cross-functional collaboration
Preferred skills
Advanced degree in health/life science, Experience with moderately complex projects
Technologies
Microsoft Word, Excel, Outlook
Responsibilities
Support study start-up activities including protocol development, IRB submissions, and site selection; Coordinate with clinical sites on administrative documentation and study materials; Maintain compliance with FDA and GCP requirements; Assist with study closeout and monitoring activities; Track study-related payments and invoices; Provide operational support for cross-functional systems and processes.
Seniority
Senior, hands-on IC
