Study Site Management Specialist
Core
Managing day-to-day execution of sponsored clinical studies at the site and regional vendor level, serving as the primary liaison for study sites, vendors, and clinical trial associates.
Role type
Study Site Management Specialist
Builds
Clinical studies for medical devices and medicines
Domain
Clinical Research Operations / Medical Devices / Pharmaceuticals
Deliverable
client delivery
Required skills
Site management coordination, vendor qualification and oversight, regulatory compliance (ICH GCP, ISO 14155), site training and quality assurance, study documentation development, budget planning and accruals, cross-functional collaboration
Preferred skills
Bachelor of Science in engineering, design, scientific, clinical, life sciences, nursing, or pharmacy; 3 years of relevant industry experience
Technologies
Study management systems
