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Clinical Research Associate Professional
7 days ago
At IQVIA Argentina, we are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a crucial role in ensuring the success of clinical trials by conducting site monitoring visits and managing study data.
Key Responsibilities:
- Perform site monitoring visits to ensure compliance with regulatory requirements and study protocols.
- Collaborate with sites to adapt and drive subject recruitment plans.
- Evaluate the quality and integrity of study site practices.
- Manage study progress by tracking regulatory submissions and approvals.
- Create and maintain documentation regarding site management and monitoring visit findings.
Qualifications:
- Bachelor's Degree in a scientific discipline or healthcare preferred.
- At least 1 year of on-site monitoring experience.
- Good knowledge of applicable clinical research regulatory requirements.
- Excellent communication and organizational skills.
