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Clinical research associate freelance

San Polo (Provincia di Venezia)
Contratto a tempo indeterminato
Libero professionista
Evidilya
Pubblicato il 12 settembre
Descrizione

Evidilya, the dedicated Contract Research Organization of Sprim Health Group operates as a full-service international expertise in successfully developing and managing observational, pre-clinical and clinical trials, is 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, close out visits, according to SOPs and study Monitoring Plan
Handle remote data monitoring using validated EDC system/software
Write Monitoring Reports and performing site management, addressing FU activities
Source Data Verification (SDV/eSDV)
Check data integrity
Support the team on the submission of the study to ethics committees/IRBs

Hard & Soft Skills:

Bachelor’s degree/MD or equivalent in technical-scientific field
Proved experience in clinical monitoring and proven trainings in the field
Proven GCP-ICH training
Actual CRA certification as per MoH decree 15/11/2011
Fluent in English
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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