Clinical research associate I or II – São Paulo/SP

Responsabilidades

• Working independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.
• Running sponsor generated queries efficiently and taking responsibility for study cost efficiency; participating in the preparation and review of study documentation and feasibility studies for new proposals as required.
• Developing and maintaining strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
• Ensuring patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory requirements.

Requisitos

• University degree in medicine, science, or equivalent.
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data.
• Excellent written and verbal communication in English.
• Good social skills enabling you to deal with queries in a timely manner.
• Ability to travel at least 60% of the time (international and domestic – fly and drive) and should possess a valid drivers license.

Marcado como: Análise de Dados, Análises Clínicas, Estudos Clínicos, Pesquisa Clínica, Pesquisa e Desenvolvimento