Client: Evidilya
Location:
Job Category:
Other
EU work permit required:
Yes
Job Reference:
8662617666420211712337132
Job Views:
3
Posted:
27.08.2025
Expiry Date:
11.10.2025
Job Description:
Evidilya, the dedicated Contract Research Organization of Sprim Health Group, operates as a full-service international organization specializing in developing and managing observational, pre-clinical, and clinical trials. We are looking for a:
Clinical Research Associate
To reinforce the Operational Italian Team.
Main Responsibilities:

Conduct and perform SQV/Pre-study Visits, site initiation visits, monitoring visits, and close-out visits according to SOPs and study Monitoring Plan.
Write Monitoring Reports and manage site activities, including follow-up activities.
Check data integrity.
Support the team in submitting the study to ethics committees/IRBs.

Hard & Soft Skills:

Bachelor’s degree/MD or equivalent in a technical-scientific field.
Proven experience in clinical monitoring and relevant training in the field.
Proven GCP-ICH training.
Current CRA certification as per MoH decree 15/11/2011.
Excellent organizational and time management skills.

Additional Requirements:

Availability to travel, especially in Central-South Italy.

What We Offer:

Full remote job.
Multicultural, young, and dynamic work environment.

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