Senior Research Associate
Core
Support clinical and basic research programs by coordinating protocol development, managing trial documentation, and facilitating patient care and data collection.
Role type
Senior Research Associate (Clinical Protocol Coordinator)
Builds
Clinical trial operations and regulatory compliance for NIH research programs
Domain
Biomedical research / Clinical trials
Deliverable
dashboards & analysis
Required skills
Protocol development, Regulatory document management, Clinical trial coordination, Data entry and database management, Staff training, Patient recruitment support
Preferred skills
Electronic Data Capture (EDC) systems, Liaising with regulatory authorities
Responsibilities
Assist researchers with protocol development and document assembly, Maintain trial documentation and study databases, Collect and submit regulatory documents to IRB, Support participant recruitment and scheduling, Train staff and investigators on protocol processes, Generate weekly progress reports
Seniority
Senior, hands-on IC