You will be responsible for 2-3 projects in CT, conduct trials in accordance with protocols. SO´Ps, local regulations and ICH-GCP guidelines including: feasibility, sites selections, obtaining necessary approvals and documentation. Other duties will be site management, data clearing activities, clause -out and archiving.
We are looking for candidates with minimum of 1 years experience in a clinical trial who is able to travel for 40% of the working time.
We offer to working in second-largest CRO in ČR, 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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