Job Description

**Experienced Clinical Research Associate, Italy**



**Your responsibilities will include:**



+ Performing site selection, initiation, monitoring and close-out visits

+ Supporting the development of a subject recruitment plan

+ Evaluating the quality and integrity of site practices in accordance with regulatory requirements, i.e., Good Clinical Practice and International Conference on Harmonization guidelines

+ Managing progress by tracking regulatory submissions, recruitment, case report form completion, and data query resolutions

+ Collaborating with experts at study sites and with client representatives



**Qualifications:**



+ University Bachelor's Degree and Master's Degree in scientific discipline or health care

+ In possession of CRA Certification as required by Ministerial Decree dated 15.11.2011

+ Experience in Pharma Industry, and/or Clinical Trials envi...

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