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
remote and on-site monitoring
regulatory documentation review
protocol conduct communication
IT applications on various devices
Nice-to-have
strong site relationships
solution-oriented approach
high quality and compliance mindset
growth mindset
culturally sensitive working relationships
customer focus commitment
Key Requirements
Associate's degree or equivalent with 3 years of healthcare experience
Bachelor's degree with 6 months of healthcare experience
Bachelor's degree non-healthcare with 2 years of healthcare experience