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Senior Study Manager Associate
Eingestellt von Real Staffing Group aus Frankfurt am Main
Projektbeschreibung
Main Responsibilities (to include but not be limited to):
+ Responsible for ensuring all site-related activities and files are completed and in line with the SOPs
+ Review of clinical data as presented via monitoring reports and data listings. Perform quality checks of all study plans and reports.
+ Responsible for collecting and tracking study specific data
+ Responsible for all tasks associated with preparation, collection, review and tracking of all documents
+ Reports any potential GCP violations and participates in any corrective/preventative action plans
+ Assists Global and Regional Study Managers with all aspects of clinical studies, from start up to close out
Skills/Experience:
+ Educated to degree level in with Science or Health-related field
+ Must have previous Clinical Research and Monitoring experience
+ Must have excellent understanding of GCP, ICH, PhRMA code and CFR Guidelines
+ Knowledge of concepts of clinical research and drug development
This is a fantastic opportunity offering the successful candidate a permanent position within a reputable organisation.To find out more about Real please visit www.realstaffing.com
Projektdetails
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Einsatzort:
Buckinghamshire, Vereinigtes Königreich
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Projektbeginn:
asap
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Projektdauer:
Keine Angabe
- Vertragsart:
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Berufserfahrung:
Keine Angabe
Geforderte Qualifikationen
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Kategorie:
Sonstiges