Offerte di lavoro per Clinical Associate Director
Ora disponibile 35 i risultati sono coerenti
Ordina per:pertinenza - Data
CLINICAL RESEARCH ASSOCIATE
Monitor site compliance with study protocol and GCP. Perform source data review and verify adequacy of clinical data through comparison of case report forms to source documents per CMP. Ensure the site is entering data according t...
Azienda | Guarda Altre Offerte |
---|---|
Indirizzo | Lazio |
Categoria | Scientifico |
Data di pubblicazione | 2 mesi fa Vedi dettaglio |
Clinical Research Associate
Guarda Altre Offerte
Lazio
Monitor site compliance with study protocol and GCP. Perform source data review and verify adequacy of clinical data through comparison of case report forms to source documents per CMP. Ensure the site is entering data according t...
2 mesi fa visto Vedi altro...
- Mostra tutto - Lavoro Lazio
Clinical Research Associate
Guarda Altre Offerte
Lazio
Monitor site compliance with study protocol and GCP. Perform source data review and verify adequacy of clinical data through comparison of case report forms to source documents per CMP. Ensure the site is entering data according t...
2 mesi fa visto Vedi altro...
- Mostra tutto - Lavoro Lazio
CRA II / Senior Clinical Research Associate - Multisponsor
Guarda Altre Offerte
Palermo, Sicilia
Conduct, drive and manage country specific feasibility and/or site pre-qualification and qualification activities, which may include: -Preparation, negotiation, and facilitation of execution of Confidentiality Agreements (CDA), Cl...
2 mesi fa visto Vedi altro...
- Mostra tutto - Lavoro Sicilia
Clinical Research Associate II - Ophthamology - Italy
Barrington James
Italy
Based on Experience
Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation...
2 mesi fa visto
Clinical Research Associate III - Ophthamology - Italy
Barrington James
Italy
Based on Experience
Clinical Trial Monitoring: Conduct site initiation, routine monitoring, and close-out visits to ensure protocol compliance and data integrity. Perform source document verification, review of case report forms, and data validation...
2 mesi fa visto