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Biotech Clinical Trials Coordinator
hace 2 semanas
Role Overview
We are seeking a highly skilled Clinical Research Associate to join our team in Argentina. As a Clinical Research Associate at IQVIA Argentina, you will be responsible for overseeing site management and monitoring activities for clinical trials across multiple therapeutics, including Oncology, Cardiovascular, Internal Medicine, and Ophthalmology.
Key Responsibilities
- Lead site management and monitoring activities to ensure compliance with study protocols, regulations, and guidelines.
- Develop and implement effective subject recruitment strategies to meet project goals.
- Provide protocol and study-related training to assigned sites and maintain open communication channels to address project expectations and issues.
- Evaluate site performance and identify opportunities for improvement to ensure high-quality trial execution.
- Track and manage study progress, including regulatory submissions, recruitment, and data queries.
- Maintain accurate records and documentation of site management activities and monitoring visit findings.
- Collaborate with study team members to provide project execution support.
- May be responsible for site financial management and invoice retrieval according to local requirements.
Requirements
- Bachelor's degree in a scientific discipline or health care field.
- At least 1 year of on-site monitoring experience.
- Equivalent combination of education, training, and experience may be accepted in lieu of degree.
