Evidenze
Biotech
ClinicalResearchAssociate(CRA)
Neural analysis suggests this role is
optimal for Mid+ candidates.
“Clinical Research Associate (CRA) at Evidenze. Skills: Clinical research, GCP compliance, Site monitoring. Ensure studies compliance. Perform site visits”
Industry & Context.
Availability to travel across Italy
What They're Looking For.
Must Have
Degree in life sciences, Certification in accordance with Italian Ministerial Decree, Knowledge of GCP, Knowledge of clinical trial regulations, Excellent English
Nice to Have
Additional languages a plus
What You'll Do.
Ensure studies compliance
Oversee patient recruitment
Manage CRF completion
Manage query management
Manage communication with vendors
Ensure accurate AE reporting
Manage protocol deviations
Maintain study documentation
Collaborate across teams
Support site payments
How You'll Work.
Team & Collaboration
Collaborate across teams
Full Job Description
Join us At Evidenze , we are committed to advancing the biomedical field and supporting healthcare professionals. Our mission is to drive meaningful innovation in healthcare, improving clinical practice and patients’ quality of life. With over 300 professionals , we deliver end-to-end solutions across clinical research, patient support programs, medical education, and healthcare communication. We’re currently looking for a proactive Clinical Research Associate (CRA) to join our Clinical Operations team in a hybrid role (Milan-based) . Prerequisite What you’ll do Ensure studies are conducted in compliance with protocols, GCP, and regulations Perform site visits (selection, initiation, monitoring, close-out) Oversee patient recruitment, CRF completion, and query management Support sites and manage communication with external vendors Ensure accurate AE reporting and manage protocol deviations Maintain study documentation and files Collaborate across teams and support site payments What we’re looking for ·Degree in life sciences (Pharmacy, Biology, Biochemistry, or related) Certification in accordance with the Italian Ministerial Decree of November 15, 2011. Strong knowledge of GCP and clinical trial regulations Excellent English (additional languages a plus) Availability to travel across Italy A dynamic, organized, and proactive mindset What we offer Permanent contract Hybrid working model Continuous training & development Competitive compensation Real career growth opportunities Supportive and collaborative environment Location: Milan HQ (Hybrid) Ready to make an impact in clinical research? Apply now or reach out to learn more! What are we expecting from you?
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