The Clinical Research Associate is responsible for managing and monitoring clinical trials to ensure they are conducted in compliance with study protocols, ICH-GCP, and applicable regulations. This includes site selection, initiation, monitoring, and close-out activities, while ensuring data quality and patient safety. The role reports to the Clinical Project Manager.
Conduct feasibility, pre-study, initiation, monitoring, and close-out visits
Ensure compliance with protocols, SOPs, ICH-GCP, and regulatory requirements
Perform source data verification and ensure data accuracy and completeness
Ensure proper reporting of adverse events and protocol deviations
Manage investigational product handling, storage and accountability
Write monitoring reports and follow-up communications
Collaborate with project teams, sponsors and site staff
Support audits/inspections and mentor junior CRAs
Degree in a scientific field
Minimum 2 years’ CRA or clinical trial monitoring experience
Strong knowledge of ICH-GCP, ISO14155, and clinical trial processes




Good English and Microsoft Office skills
We offer a competitive salary with other benefits/bonuses and opportunity to develop your professional career with an expanding and growing company.
Founded in 1998 in Italy and now operating at an international level, OPIS is a full‑service science‑driven biotech focused CRO providing premium trial management for multi‑country clinical trials, including state‑of‑the‑art information technology solutions and innovative approaches to the increasing complexity and variety of current projects. OPIS added value lies in its highly specialized professionals who can assist their clients using their deep know‑how and experience to guarantee a top‑quality level of Clinical Trial Management and ability to operate in a wide range of fields (medical writing, scientific and statistical consultancy for trial design, regulatory activities, pharmacovigilance, etc.)

📌 Research Associate (Italia)
🏢 Opis
📍 Italia