Research Associate, Buenos Aires, IQVIA Team Member
hace 5 días
About the Job
This Clinical Research Associate position is available in our Buenos Aires office. The successful candidate will be responsible for performing site monitoring visits to ensure compliance with Good Clinical Practice (GCP) guidelines and managing study progress by tracking regulatory submissions and approvals.
Responsibilities
- Perform site monitoring visits to evaluate site practices and ensure compliance with GCP guidelines.
- Work with sites to adapt and track subject recruitment plans.
- Administer protocol training to assigned sites.
- Evaluate the quality of site practices related to the proper conduct of the protocol.
- Manage study progress by tracking regulatory submissions and approvals.
- Establish regular communication with sites to manage ongoing project expectations and issues.
Requirements
- Bachelor's Degree in a scientific discipline or healthcare preferred.
- Requires at least 1 year of on-site monitoring experience.
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