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- Bachelor's degree or equivalent in appropriate scientific or business disciplines; familiar with relevant ICH/GCP, EU and FDA guidelines and SOPs;
- 8-10 years of experience in clinical operations; specifically with adoption management of eTMF CTMS systems associated processes;
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clinical trials specialist - Roma - beBeeMedicines
Titolo del lavoro: Clinical Trial Documentation
Descrizione
Job Title
Clinical Trial Documentation and Records Management Lead
About the Role
This is a critical role in ensuring the success of our clinical trials. The successful candidate will be responsible for leading a team of professionals to manage all aspects of clinical trial documentation and records management.
We are looking for an experienced professional who can lead our team effectively while possessing excellent knowledge healthcare compliance regulations guidance.
Benefits, This company offers dynamic working environment flexible hybrid arrangements that promote work-life balance across organization worldwide people-care services available including tax assistance relocation support remote working benefits access numerous learning training opportunities aligned continuous growth professional wellbeing . ', '', «You would join fast-growing friendly community where we invest continuously train learn develop teams,¬ ….“We strive satisfy needs quality well-being aiming come happy day.” Flexible Working Approach Remote Work , Support Relocation Process Tax Assistance Service Foreign Colleagues Many Other People-Care Services , Seniority Level Mid-Senior Employment Type Full-time Job Function Research Pharmaceutical Manufacturing-', '', '
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Data Acquisition Expert
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Clinical Specialist Biosurgery
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Product Support Specialist Joint Replacement – Center Italy
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Fishery Resources Specialist
Solo per membri registrati Rome
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Chief Evidence for Development Impact and Innovation Unit
Solo per membri registrati Roma
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Clinical Specialist, Triveneto
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