$31.51 - $62.64 hourly; not specified; not specifi...
On-site
Regulatory coordination
Clinical research studies
Irb submissions
The Study Activation Coordinator provides comprehensive regulatory coordination for clinical research studies across assigned units, departments, or divisions
Job Summary
The Study Activation Coordinator provides comprehensive regulatory coordination for clinical research studies across assigned units, departments, or divisions.
This role is responsible for study regulatory activities for study activation, ensuring strict adherence to federal, state, sponsor, and institutional requirements.
The position also supports quality assurance and audit readiness activities, maintains documentation within the Clinical Research Management System (CRMS), and proactively applies evolving regulatory knowledge to ensure continuous compliance.
Matching Summary
The Study Activation Coordinator provides comprehensive regulatory coordination for clinical research studies across assigned units, departments, or divisions.
Salary
$31.51 - $62.64 Hourly; Not specified; Not specified
Skills & Requirements
Must-have
regulatory coordination
clinical research studies
IRB submissions
FDA submissions
sponsor requirements
Nice-to-have
interpersonal skills
analytical skills
attention to detail
learning mentality
Key Requirements
Bachelor's degree or equivalent experience
1+ years clinical researcher experience
Proficiency with Adobe and Microsoft suite
Working knowledge of clinical research regulations