Clinical Research Associate, Site Management - Italy
IQVIA
Milan, Italy
Good clinical practice (gcp)
Ich guidelines
Protocol requirements
Engage in structured training to gain knowledge and skills required to independently conduct clinical monitoring visits
Job Summary
Engage in structured training to gain knowledge and skills required to independently conduct clinical monitoring visits.
Under close supervision, perform site monitoring visits (selection, initiation, monitoring and close out visits) in accordance with contracted scope of work and good clinical practices.
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, CRF completion and submission, and data query generation and resolution.
Matching Summary
Engage in structured training to gain knowledge and skills required to independently conduct clinical monitoring visits.
Skills & Requirements
Must-have
Good Clinical Practice (GCP)
ICH guidelines
protocol requirements
site monitoring visits
TMF filing
Nice-to-have
therapeutic training
recruitment plan development
effective time management
client relationship building
Key Requirements
Bachelor's Degree in scientific discipline or health care
Local ministerial decree requirements
1 year prior clinical experience preferred
Proficiency in Microsoft Office Suite
Good command of English language
Work Rights
In possession of local ministerial decree requirements as per Italian law