Senior Clinical Research Associate (CRA)
iqvia · Buenos Aires
Job description
About the role
The Senior Clinical Research Associate will lead site selection, initiation, monitoring and close‑out activities for clinical trials, ensuring data integrity and regulatory compliance.
Key responsibilities
- Perform site selection, initiation, monitoring and close‑out visits while maintaining complete documentation.
- Develop and support subject recruitment plans and provide protocol training to sites.
- Evaluate site practices, escalate quality issues, and track regulatory submissions, recruitment, CRF completion and data queries.
Required profile
- Bachelor’s degree in a health‑care or scientific discipline (or equivalent).
- Minimum 4 years of on‑site monitoring experience.
- Advanced English proficiency and strong organizational, communication and interpersonal skills.
Required skills
- In‑depth knowledge of Good Clinical Practice (GCP) and ICH guidelines.
- Proficiency with Clinical Trial Management Systems (CTMS) and Electronic Data Capture (EDC) systems.
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Published 9 hours ago
Expires 1 month from now
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iqvia
Buenos Aires