Contrato de Trabalho - Clinical Research Associate
Perform all types of site visits including, but not limited to, qualification visits, initiation visits, monitoring visits, motivational visits, audit support visits, and termination visits, ensure that all study related communication including e-mail is tracked, printed and filed as required, to track patient recruitment by contacting investigators as specified for the study, to assemble files and ensure documents for the trial master file accurately reflect the progress of the study and other Ad-Hoc CRA duties.
Área Científica: Biomedicina ou relacionada
Local: Lisboa - See map
Habilitações: Licenciatura
Experiência: previous CRA experience within clinical research of approximately 2 years, good clinical knowledge with an understanding of medical terminology, understanding of the principles of ICH GCP and regulatory requirements, experience using a clinical trial management system, preferable experience using a clinical trial management system (CPMS) and experience as a CRA on single site and/or multicentre trials.
Início: -
Duração: contrato
Montante: -
Abertura Concurso: 15 de Maio de 2017
Montante: -
Abertura Concurso: 15 de Maio de 2017
Deadline: CLOSED
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