SENIOR SITE MANAGER
Core
Primary contact between Sponsor and Investigational Site ensuring inspection readiness and compliance with clinical trial protocols, SOPs, and GCP from start-up to closure.
Role type
Senior Site Manager (Clinical Trial Support)
Builds
Clinical trial operations at assigned sites
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
GCP compliance, site monitoring (on-site and remote), subject recruitment and retention planning, data management, adverse event reporting, supply chain management, regulatory documentation, therapeutic area knowledge
Preferred skills
Process improvement, mentoring, site selection assistance, investigator meeting presentation
Technologies
Company trial management systems, reporting dashboards
Responsibilities
Execute site initiation, monitoring, and close-out activities; ensure staff training and data accuracy; manage clinical drug supplies; report Adverse Events; prepare for audits and inspections; track site-level costs; mentor less experienced managers
Seniority
Mid-level, operates independently with little supervision
