CLINICAL RESEARCH ASSOCIATE/HALF-TIME JOB/HOME BASED/ONLU
2011-08-16
Our client is a local CRO and we are looking for new member for the clinical trial team.
You will responsible for selection process, conduct pre-study visits, check suitability of chosen sites before study allocation, Complete study documentation, Submit CTA to SUKL for opinion and obtain ECs approval. Attend monitors meeting before study start. Together with study manager you will responsible for organization of Investigators start up meeting, if held locally, or arrange logistic for Czech sites participants if held internationally. Check quality of centres work including CRF completion within requested timelines.
After study completion is responsible for study closure visits conduct, archiving according appropriate SOPs including preparation of local archived documentation and organizing documents at electronic folder. Participation or organization of final meeting, if planned
Ideal candidates will have minimum of 2 year experience as a CRA. English communication ability.
We offer to working home based, total rewards package which includes competitive compensation, excellent benefits, and career and development opportunities.
In case of interest please send your CV to Lucie Ondruchova, ondruchova@hays.cz
