Clinical Research Associate
Core
Conduct independent site feasibility, selection, initiation, and monitoring for clinical trials and exploratory research projects.
Role type
Clinical Research Associate
Builds
Clinical trial data and regulatory compliance for exploratory research projects
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Good Clinical Practice, Pharmacology, Regulatory affairs, Clinical trials, Site monitoring
Responsibilities
Carry out independent site feasibility and selections; Help with site initiation and trial activation; Carry out independent site monitoring (online and offline); Help with preparing Serious Adverse Event report filing; Provide assistance to site in protocol related queries; Conduct ICH GCP Training for site personnel; Act as liaison between sponsor, investigator, and CRO; Support site preparation for regulatory audit and inspections