Clinical Research Associate

Location: Sant'Ambrogio di Torino

Company Description
Phidealive, established in 2018, is a Contract Research Organization (CRO) with a strong foundation in Italy’s rich clinical research culture. Positioned as a Clinical Research Atelier, Phidealive emphasizes scientific rigor, regulatory compliance, and a tailored operational approach for each project. The company collaborates with Pharma, Biotech, Medical Device, Food Supplement, and Cosmetic companies on complex national and international research initiatives. With a multidisciplinary and distributed team, Phidealive is committed to transparency, ethical responsibility, and exceptional quality in its services.

Role Description
This is a full-time Hybrid role for a Clinical Research Associate, based in Milan. The Clinical Research Associate will monitor and manage clinical trials, ensure adherence to study protocols, conduct site visits, and verify data accuracy and regulatory compliance. Responsibilities include collaborating with clinical operations teams, maintaining effective communication with study sites, and supporting research activities to achieve project objectives.

ONLY CV WITH DM 15/11/11 CERTIFICATION AND PROVEN EXPERIENCE AS CRA (MINIMUM 3 VISIT IN AUTONOMY ) WILL BE TAKEN INTO CONSIDERATION.

Qualifications
Proficiency in Clinical Research Associates’ responsibilities, including site monitoring, documentation, and compliance with trial guidelines.
Experience in designing and executing study protocols and managing clinical trials.
Strong knowledge of Clinical Operations and Research methods, ensuring effective trial execution and data analysis.
Keen attention to detail, excellent organizational skills, and ability to work effectively in multidisciplinary teams.
A Bachelor’s or Master's degree in Life Sciences, Health Sciences, or a related field is required.
Working knowledge of relevant clinical trial regulations and guidelines, including ICH-GCP standards.

Experience of monitoring in interventional studies
Proven experience in Oncology, Cardiovascular, CNS and Rheumatology therapeutic areas is preferred
Prior experience within a CRO environment is an asset.
Proficiency in spoken and written English and Italian.