Clinical Research Associate - Hungary Nr ref.: /JOBS.pl My client are a globally recognised outsourcing CRO, contributing to studies on a global scale. This is a fantastic opportunity for an experienced CRA to join a rapidly expanding clinical team and progress in his/her career. The positions offer the opportunity to work office-based in Budapest for 3 months and then fully home-based on a full-time, permanent basis. Responsibilities Include: · Assisting in protocol writing/review. · Prepare and conduct all site monitoring visits, from study start-up to close-out according to relevant SOPs. · Assist in the writing, review and tracking of CRFs collected during monitoring visits. · General assistance activities reporting to the Project Manager/ Lead CRA. The degree of responsibility given to the successful candidate shall reflect his/her experience and the level of contribution, which he/she can make to that project. The salaries and benefits packages will be judged on a similar basis. Requirements · Demonstrated experience as an independent monitor in multicentre studies. · Demonstrated experience of Oncology-related Clinical Trials (Phases II and III) is preferred. · Preference for candidates who have a BSc or BA degree in Biomedical or Life Sciences. If you would like to find out more about the company and the role, please send an up-to-date CV to or call for a confidential discussion. CRA, Senior CRA, Monitoring, Monitor, Feasibility, Start-up, Cardiovascular, Cardiology, Close-out, Senior Monitor, Clinical Research, Oncology, CRO, Pharma, Pharmaceuticals, Clinical Trials, On-Site, Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .
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