CRA Clinical Research Associate

Perform and coordinates all aspects of the clinical monitoring and site management process in accordance with ICH, GCP, FDA guidelines, local regulations and PPD SOPs. Conducts site visits to assess protocol and regulatory compliance and manages required documentation responsible for ensuring that data will pass international quality assurane audits.

Bachelors degree in a science related field or a Registered Nursing certification or equivalent certification/licensure from an appropriately accredited institution.

Previous experience as a clinical research monitor that provides the knowledge, skills, and abilities to perform the job.

Good English Language and grammar skills.

Proven clinical monitoring skills.

Empresa: PPD Mexico, S.A.de C.V.
Localidad: Guatemala (Extranjero)
Sector: Salud
Profesiones relacionadas: No indicado
Tipo de contrato: Temporal, Jornada Completa
Experiencia mínima: 2 años
Fecha de publicación: 11-01-2010
Salario: No especificado

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