Cra

3 settimane fa


Roma, Italia CliniRx A tempo pieno

At Clini Rx, we are committed to delivering high-quality clinical trial solutions with precision, integrity, and innovation. We're looking for a Clinical Research Associate (CRA) who shares our passion for excellence and is ready to make a real impact in advancing clinical research. What You'll Do: Drive the site monitoring plan by ensuring timely, high-quality delivery in alignment with protocol, SMMP, and project plans. Conduct site initiation, monitoring, and closeout visits , ensuring all activities comply with SOPs and regulatory requirements. Perform Source Document Verification (SDV) , review ICFs, oversee e CRF completion, and ensure SAE reporting accuracy. Collaborate with investigators to ensure adherence to protocols, regulatory guidelines, and ICH GCP standards. Support sites with training, essential document collection, and audit/inspection readiness. Identify and engage potential new sites across therapeutic areas. Who You'll Work With: You'll collaborate closely with our Project Managers, Clinical Operations team, site personnel, and QA teams to ensure seamless study delivery. What Success Looks Like: High-quality and timely site monitoring Accurate and compliant documentation Strong site engagement and smooth study execution What We're Looking For Graduate/Postgraduate in Life Sciences 1–4 years of experience in site monitoring Strong knowledge of ICH GCP and clinical trial regulations Excellent communication, multitasking, and problem-solving skills Location: 100% Remote (Home-Based) At Clini Rx, we believe in empowering our people and creating opportunities to grow while making a meaningful difference in global healthcare. If you're ready to contribute to impactful clinical research and grow with a collaborative team, apply now.


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