Experienced Bilingual Clinical Research Associate (cra Ii, Sr Cra, Pcra) - Montreal, Qc
PPD (Thermo Fisher) UK
Montreal, Quebec, Canada
Remote
Risk-based monitoring approach
Ich-gcp guidelines
Site processes specialist
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation
Job Summary
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.).
You will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
Matching Summary
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
Skills & Requirements
Must-have
risk-based monitoring approach
ICH-GCP guidelines
site processes specialist
remote or on-site visits
protocol and regulatory compliance
Nice-to-have
root cause analysis
critical thinking and problem-solving skills
collaborative relationships with investigational sites