Our client is Clinical Research Organization and we are looking for new member for our Prague office. You will report to Generel Manager Czech Republic & Slovakia. You will be responsible for Clinical studies. Ensuring management of trials is done in compliance with ICH, GCP. Ensuring clinical trials are effectively executed and completed within budget, timelines and meeting enrolment commitments as well as routine updating of CTMS and other clinical systems. Manage site pre-selection and validation process. Support local investigator meetings, ensure contracts and applicable reg documentation is obtained prior to study start.
Ensure clinical study site close-out in accordance with local regulations and ensure dissemination of clinical trial results to the participating study investigators.
Ideal candidates will have minimum of 5 years experience in clinical research, experience in a monitor role or role overseeing clinical trials, strong project Management and leadership sills.
We offer to working in international company total rewards package which includes competitive compensation, excellent benefits, and career and development opportunities.
In case of interest please send your CV to Lucie Ondruchová at ondruchova@hays.cz
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