Relocation Support: This role is based in Buenos Aires, Argentina. Novartis is unable to offer relocation support: please only apply if accessible.
Take the next step in your clinical research career by leading the delivery of complex trials that make a meaningful difference to patients. As an Expert Clinical Research Associate at Novartis, you will serve as a trusted partner to investigative sites, driving performance, quality, and compliance across Phase I to Phase IV studies. In this highly collaborative and dynamic role, you will leverage your expertise to manage site relationships, proactively identify risks, and support the successful execution of innovative clinical trials while contributing to the development of peers and the advancement of clinical operations excellence.
Job Description
Key Responsibilities
- Lead site relationship management to support successful execution of Phase I through Phase IV trials
- Serve as the frontline liaison between Novartis and assigned investigative sites
- Manage complex study sites according to monitoring plans, procedures, and regulatory requirements
- Conduct site initiation visits and ensure site staff are trained on trial requirements
- Perform ongoing onsite and remote monitoring to ensure compliance and data integrity
- Identify site risks, process gaps, and improvement opportunities to support trial quality
- Promote a strong compliance culture focused on patient safety and ethical trial conduct
- Partner with cross-functional stakeholders to support recruitment, site development, and data quality
- Support audit and inspection readiness, including timely implementation of corrective actions
- Mentor junior Clinical Research Associates and contribute to innovative monitoring practices
Essential Requirements
- Degree in a scientific or healthcare discipline (or, for United St
📌 Expert Clinical Research Associate (Ramallo)
🏢 Novartis
📍 Ramallo
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