Clinical research associate

  • Pubblicato il 08/07/2026
  • Turbigo (MI)
  • Da definire
  • 70000

Descrizione:

Freelance Clinical Research Associate – ALS Study – Strong monitoring experience Upsilon Global is seeking an experienced freelance Clinical Research Associate (CRA) to support an active ALS study based in Italy. This is a pivotal role within a busy clinical research environment and requires a CRA with strong monitoring experience, organisational skills, and the ability to work autonomously across study activities. You will work closely with the sponsor, investigators, and site teams to ensure the successful delivery of the study while maintaining high‑quality standards and compliance with ICH‑GCP guidelines. This is a fantastic opportunity for someone with strong site management and communication skills to have a direct impact on study delivery within an ALS research setting. Key Information Position: Clinical Research Associate (Freelance) Location: Milan, Italy FTE: 0 (Full‑time equivalent) Start Date: As soon as possible Duration: Initial contract with potential extension Responsibilities Conduct site monitoring visits, including Site Initiation Visits (SIVs), Interim Monitoring Visits (IMVs), and Closeout Visits (COVs). Ensure sites remain compliant with protocol, ICH‑GCP, and regulatory requirements. Verify source data and review study documentation. Support site staff with study conduct and query resolution. Ensure timely data entry and resolution of outstanding queries. Review and track safety reporting and essential documents. Support recruitment and patient retention activities. Maintain strong communication with sponsors and investigative sites. Qualifications Prior CRA experience within clinical research, preferably Oncology or Hematology; experience in ALS or neurology is advantageous. Strong understanding of ICH‑GCP and clinical trial processes. Experience with Electronic Data Capture (EDC) systems and study documentation review. Ability to work independently and manage multiple sites effectively. Strong organisational and communication skills. Experience working within a fast‑paced clinical research environment. This role would be well suited to an experienced CRA with a proactive approach and strong relationship‑management skills. #J-18808-Ljbffr