Acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites
Job Summary
Acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.
Performs clinical study site management/monitoring activities in compliance with ICH-GCP, Sponsor SOPs, Local Laws & Regulations, Protocol, Site Monitoring Plan and associated documents.
Manages and maintains information and documentation in CTMS, eTMF and various other systems as appropriate and per timelines.
Matching Summary
Acts as primary site contact and site manager throughout all phases of a clinical research study, taking responsibility of allocated sites.
Skills & Requirements
Must-have
ICH-GCP compliance
site management activities
protocol conduct communication
regulatory documentation review
data accuracy and integrity
site performance problem resolution
Nice-to-have
customer focus
positive mindset
growth mindset
conflict management skills
culturally sensitive working relationships
Key Requirements
3 years relevant healthcare experience (Associate's degree)