From this position, you will participate in the nomination of appropriate investigational sites for clinical trials (phase IV), while also organizing, managing and monitoring them. You will act as the central point of communication between Novartis and Investigators for all trial-related activities and ensure that trials are conducted on time and budget, and fully GCP, ICH and Novartis SOP compliant.
To join this opportunity, you should have studies in Life Sciences and 1-2 years of professional experience in clinical research, ideally with phaseIV trials. You should also possess knowledge and experience in international standards (GCP/ICH) and local regulations.
Strong communication and organizational skills are necessary as well as demonstrated ability to work in teams and take the lead in group activities. PC literacy and fluency in English are essential.
If you are interested in the role, please submit your resume at hr.novartishellas@novartis.com with reference code (CRA).
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