CLINICAL RESEARCH ASSOCIATE
Descrição da oferta de emprego
Main responsibilities.
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation Supporting the development of a patient recruitment plan Establishing regular lines of communication plus administering protocol and related study training to assigned sites Evaluating the quality and integrity of site practices – escalating quality issues as appropriate Tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution Background.
Bachelor’s degree in a health care or other scientific discipline or educational equivalent At least 2 years of on-site monitoring experience Fluent English and another European language Please note, this role is for pipelining reasons.
Detalhes da oferta
- Actalent
- Em todo Portugal
- Indeterminado - Indeterminado
- Indeterminado
- 15/05/2023
- 14/06/2024
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