Becas Monitor de Ensayos Clinicos GCO 2017 1

Descripción de la oferta

· Help LTM/SM in ensuring that the current versions of the required trial documents, trial-related materials and supplies are provided to the investigational site.
· Support the LTM or the SM in ECs and Health Authorities Submissions.
· Help the SM in obtaining site related trial documents.
· Support the LTM/SM in collecting and processing as appropriate the IFDF, the 1572 forms and related documents throughout the trial.
· Assist the LTM/SM in conducting local investigator meeting or in making arrangements for the investigators participating in an international meeting as applicableHelp in the distribution, collection, reviewing, and tracking of regulatory documents, agreements and training documentation.

Perfil buscado

Estar Cursando Master de Ensayos Clínicos y poder firmar convenio de colaboración
Inglés