
Senior CRA for Clinical Trials
2 days ago
About the Position
IQVIA Argentina is seeking an experienced Senior CRA to join our site management team. As a key contributor, you will play a vital role in ensuring the successful execution of clinical trials.
Responsibilities
- Monitor site performance against study protocols and regulatory requirements.
- Partner with sites to identify opportunities for process improvements and optimized study execution.
- Deliver comprehensive protocol and related study training to assigned sites, fostering strong relationships and open communication.
- Investigate and resolve quality issues promptly, escalating concerns to relevant stakeholders as necessary.
- Manage study timelines, coordinating regulatory submissions, subject recruitment, and data collection efforts.
- Maintain accurate records of site documentation, ensuring Investigator's Site File (ISF) compliance with GCP and local regulations.
- Document site management activities, findings, and actions taken through regular reports and correspondence.
- Support project execution through collaboration with study teams.
- Apply analytical and problem-solving skills to drive site financial management and invoice retrieval.
Requirements
- Bachelor's Degree in a scientific discipline or healthcare, with preference given to candidates with clinical research experience.
- A minimum of 3 years' experience in on-site monitoring, with a strong understanding of GCP and ICH guidelines.
- Familiarity with Microsoft Office tools and proficiency in using laptop computers and mobile devices.
- Excellent written and verbal communication skills, including fluency in English.
- Proven ability to establish and maintain effective working relationships with colleagues, managers, and clients.
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