Clinical Research Associate

Company Description

PHIDEALIVE Srl is a Clinical Research Atelier and full-service Contract Research Organization (CRO) that collaborates with sponsors, biotech innovators, and investigators to design and deliver high-quality clinical studies. With a multidisciplinary team skilled in applying scientific rigor, regulatory compliance, and customized operational planning, PHIDEALIVE focuses on complex programs in the Pharma, Biotech, Medical Device, and Food Supplement sectors, as well as Investigator-Led studies. The company's mission is to produce evidence that not only exists but supports impactful, real-world decisions. Headquartered in Milan, PHIDEALIVE is committed to excellence and innovation in advancing clinical research.

Role Description

This is a full-time hybrid role for a Clinical Research Associate based in Milan, with flexibility to work partially from home. The Clinical Research Associate will be responsible for monitoring clinical trials, ensuring compliance with regulatory standards, and collaborating with sponsors, investigators, and the clinical team. The role includes planning and executing study protocols, overseeing clinical operations, managing research data, and ensuring that clinical trials are conducted in alignment with the highest levels of accuracy, quality, and ethical standards.

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

Qualifications

• DM 15/11/11 CERTIFICATION

• Proficiency in Clinical Trials, including planning, monitoring, and execution
• Experience in Clinical Research Associates tasks and responsibilities
• 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.

• Strong knowledge of Protocol and methodology relevant to clinical studies
• Expertise in Clinical Operations processes and regulatory compliance
• Ability to conduct in-depth Research and analyze clinical data effectively
• Excellent communication, organizational, and problem-solving skills
• Bachelor’s degree in Life Sciences, Medicine, Pharmacy, or a related field
• Professional proficiency in English; knowledge of Italian is a plus
• Ability to travel within Italy as required for site visits and meetings