Clinical Research Associate I
On-siteSão Paulo, São Paulo, Brazil
Job Summary
Coordinate all activities for setting up and monitoring clinical studies, including completing accurate status reports and maintaining documentation. Run sponsor-generated queries efficiently, manage study cost efficiency, and prepare feasibility studies for new proposals. Develop relationships with clinical investigators and site staff while ensuring patient safety through compliance with protocols and regulatory requirements. Requires a university degree in medicine or science, knowledge of ICH-GCP guidelines, and approximately 60% travel. Based in São Paulo or Rio de Janeiro for ICON, a global healthcare intelligence organization.
Required Qualifications
- University degree in medicine, science, or equivalent
- Knowledge of ICH-GCP guidelines
- 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
- Willingness to travel as required (approximately 60%)
- Legal right to work in the country where the role is based
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