- Acknowledge and follow company quality management systems, ICH GCP guidelines, and local/international legislation. Ensure compliance with all amendments or updates.
- In case of deviations from approved protocol/ICH GCP/guidelines/laws during study conduct, report to Line Manager according to SOPs.
- Conduct pre-study visits at potential sites for feasibility/studies evaluation resources/facilities assessment.
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· Kymos Group · KYMOS GROUP is a medium-size and fast-growing Contract Research Organization (CRO) with headquarters in Spain and laboratories in Spain, Italy, and Germany and a Liasson office in South Korea, offering comprehensive bioanalytical and CMC analytical services to th ...
Ancona (Italia)4 giorni fa
Clinical Research Associate - Ancona - Veeda Lifesciences
Descrizione
Clinical Research Associate Role at Veeda Lifesciences
Job Summary:
A Clinical Research Associate (CRA) is required to ensure the conduct of clinical trials at selected Investigational Sites adheres to approved protocols, ICH GCP guidelines, and applicable laws and regulations.
Main Responsibilities:
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Impurities Identification
Solo per membri registrati Ancona (Italia)