Social network you want to login/join with: Clinical Research Associate FREELANCE, Prato
Client:
Evidilya Location:
Prato, Italy Job Category:
Other EU work permit required:
Yes Job Reference:
8662617666420211712337140 Job Views:
3 Posted:
27.08.2023 Expiry Date:
11.10.2023 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 the study Monitoring Plan. Write Monitoring Reports and perform site management, including follow-up activities. Check data integrity. Support the team in the submission of 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 and South Italy. What we offer:
Full remote work opportunity. Multicultural, young, and dynamic work environment.
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📌 Clinical Research Associate FREELANCE
🏢 Altro
📍 Prato