Key Accountabilities:
- Build relationships with investigators and site staff. - Perform on site visits and inspects, also makes reports in accordance with the monitoring plan.
- Monitor patient safety on-site.
- Responsible for the completeness and quality of the on-site files.
- Respond to site issues alerted by the project.
- Collect study documents during site visits as needed and other work-related activities.
Desired skills and knowledge:
- University degree in held-related field.
- Knowledge of the local and international regulations related to Clinical research and GCP.
- 3 years of experience as CRA working in Oncology studies (mandatory).
- Excellent command on English.
Fecha*:
24 de Junio de 2013
Localidad*:
Lima
Departamento*:
Lima
Salario:
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Comienzo*:
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Duración*:
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Tipo de trabajo*:
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Solicitudes*:
Those interested send your CV. to e-mail: seleccion.laboratorio@hotmail.com
