Responsabilità

The CRA/CRC is responsible for the monitoring or auditing of all activities subject to the, “Buona pratica clinica ICH: Linee guida consolidate,” (GCP), supportare i programmi dei clienti gestiti da Watermark garantisce che i dati del progetto e le dichiarazioni di sintesi siano di qualità nota e documentata.

Requisiti

Will be expected to travel extensively to study sites in the US to monitor our clinical and outcome studies.
Successful applicant must have previous experience monitoring clinical trials.
Basic knowledge of worldwide regulatory requirements and/or pharmaceutical development practices.
Knowledge/understanding of the approach and perspectives of regulatory agencies.
Essential Skills and Abilities

Good written and verbal communication skills, demonstrated ability to function effectively with all levels of management
Strong negotiation and relationship building skills
Good understanding of medical / corporate governance principles
Detailed oriented and organized


NBScienza

organizzazione di ricerca a contratto

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