Senior CRA1
Core
Senior Clinical Research Associate I performing site monitoring and management to ensure clinical studies adhere to protocols and regulations.
Role type
Senior IC clinical research associate (site monitoring)
Builds
Clinical studies for life sciences and healthcare industries
Domain
Clinical research / Healthcare
Required skills
Site monitoring, subject recruitment, protocol adherence, regulatory compliance (ICH-GCP), data quality verification, TMF/ISF management, financial management support
Preferred skills
Therapeutic knowledge, Microsoft Office proficiency, English fluency
Responsibilities
Perform site monitoring visits (selection, initiation, monitoring, close-out), drive subject recruitment plans, administer protocol training, evaluate site practices, track regulatory submissions and enrollment, maintain TMF and ISF, create monitoring documentation, support start-up and financial activities
Seniority
Mid-level, hands-on IC
