The Clinical Research Associate (CRA) ensures the successful and compliant execution of clinical trials at study sites. Responsibilities include on-site and remote monitoring activities across all phases (I-IV) of GDD trials within the country, in accordance with ICH/GCP guidelines, local regulations, and SOPs.Key duties involve proactive site performance management focusing on recruitment and quality, serving as the primary contact for sites, and ensuring effective collaboration. The CRA manages assigned study sites, conducts site initiation visits, provides ongoing training, and monitors compliance with protocols and regulations. They identify process deficiencies, promote a culture of compliance and ethical integrity, and work closely with site staff to optimize patient recruitment and data quality.Additional responsibilities include site closeout activities, collaboration with project teams, participating in audits and inspections, and ensuring documentation standards are met. The role requires a degree in scientific disciplines, at least 1 year of CRA experience in pharma or CRO, fluency in Italian, good English skills, and willingness to travel across Italy.Join Novartis to contribute to innovative medicines that improve lives, supported by a diverse and inclusive work environment. Candidates interested in future opportunities can join the Novartis Network or talent community to stay connected.
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