Clinical Research Associate
6 days ago
Job Overview
IQVIA Argentina is seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for conducting site monitoring visits to ensure that sites are conducting studies and reporting data as required by the study protocol, regulations, and sponsor requirements.
Key Responsibilities:
- Perform site monitoring visits to ensure compliance with contracted scope of work and Good Clinical Practice.
- Work with sites to develop and track subject recruitment plans to enhance predictability.
- Administer protocol training to assigned sites and establish regular communication lines to manage ongoing project expectations and issues.
- Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to regulations.
- Manage study progress by tracking regulatory submissions, case report form completion, and data query generation and resolution.
- Ensure documentation is maintained in accordance with GCP and local regulatory requirements.
Qualifications:
- Bachelor's Degree in a scientific discipline or healthcare preferred.
- At least 2 years of on-site monitoring experience.
- Good knowledge of clinical research regulatory requirements and GCP guidelines.
- Excellent communication, organizational, and problem-solving skills.
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