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Clinical Research Associate
hace 2 meses
Job Overview
We are seeking a highly skilled Clinical Research Associate to join our team at IQVIA Argentina. As a Clinical Research Associate, you will be responsible for ensuring the quality and integrity of study site practices related to the proper conduct of clinical trials.
Key Responsibilities
- Site Monitoring
- Perform site monitoring visits to ensure compliance with study protocols, regulations, and sponsor requirements.
- Evaluate the quality of study site practices and escalate any quality issues as necessary.
- Manage the progress of assigned studies, including tracking regulatory submissions and approvals, recruitment and enrollment, and data query generation and resolution.
- Collaborate with study team members to ensure project execution support.
- Create and maintain accurate documentation regarding site management, monitoring visit findings, and action plans.
- Submit regular visit reports and generate follow-up letters as required.
- Bachelor's Degree in a scientific discipline or healthcare preferred.
- At least 5 years of on-site monitoring experience.
- Good knowledge of clinical research regulatory requirements, including Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
- Excellent communication and organizational skills.
What We Offer
As a Clinical Research Associate at IQVIA Argentina, you will have the opportunity to work on a variety of clinical trials and contribute to the advancement of medical research. We offer a competitive salary and benefits package, as well as opportunities for professional growth and development.
