Clinical Data

Chiesi Global Rare Diseases is seeking a Clinical Data Innovation Manager to define and execute a strategic data innovation roadmap across its rare disease portfolio. You will drive AI, automation, advanced analytics and modern data management practices to accelerate development, improve data quality, and enhance regulatory readiness. You will bridge...

Recordati is seeking a skilled Statistical Programmer to drive the programming of outputs (tables, listings, figures) and build SDTM/ADaM datasets for clinical studies. The role involves collaborating with statisticians, data managers, and safety teams to ensure CDISC-compliant deliverables and robust validation of programming utilities. Ideal candidates...

Recordati is seeking a Senior Biostatistician to provide expert statistical support across the development portfolio, including analyses for studies, integrated summaries and regulatory submissions. The role requires hands-on SAS and strong collaboration with Medical Writing and CRO partners. You will contribute to statistical strategy, ensure high...

ICON Strategic Solutions is seeking a Clinical Trial Associate to support the design and analysis of clinical trials in a sponsor-dedicated model.La preghiamo di verificare di possedere il livello di esperienza e le qualifiche adeguate leggendo la panoramica completa di questa opportunità qui sotto.You will assist with trial coordination, documentation, and...

IQVIA LLC is seeking a Clinical Research Associate to monitor study sites and ensure data reported aligns with protocol and regulatory requirements. You will manage site communications, train staff, and track regulatory submissions, recruitment, and data queries.Milano-based, onsite role requiring strong English communication and organized project oversight....

ICON Strategic Solutions is seeking a Clinical Research Associate II to design and analyze clinical trials, ensuring data integrity and patient safety across sponsor-driven studies. You will monitor sites, review data, and contribute to study documentation, working with investigators and staff to maintain high-quality trial conduct.Ideal candidates have a...

Provide support to Clinical Affairs team to assure study site selection and conduct of the study by study sites in compliance with Good Clinical Practices, federal regulations, and Clinical Affairs SOPs through in-house and some on-site monitoringConduct pre-study visits to assure the site has adequate facilities, staff, and subject population for conducting...

At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide. As a...

## Clinical Research AssociateApply: Milan: Full time: Posted Today: R36982BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our passionate...