Experteer Overview

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In this Global CRA role, you ensure oncology trials are conducted according to protocol, SOPs, GCP, and regulatory requirements to protect participants and guarantee data quality. You work across Madrid with cross-functional teams to monitor multiple sites, manage complex study designs, and oversee recruitment and data integrity. Your work supports pivotal oncology studies and drives compliant, high-standard clinical research. You will grow responsibilities as you master new tools and processes.

Compensaciones / Incentivos
• ensure trials are conducted, documented, and reported per protocol, SOPs, GCP, and regulatory requirements
• monitor oncologic patients across multiple clinical trials
• oversee monitoring of Phase 2-3 and pivotal studies; manage complex designs including SIVs




• supervise a substantial number of sites and subjects
• address protocol deviations or compliance issues and communicate with investigators
• coordinate monitoring activities during recruitment phase
• maintain proactive site and data quality oversight

Responsabilidades
• 3-4 years as CRA
• at least 2 years oncology experience
• extensive experience monitoring oncologic patients across multiple trials
• monitoring experience xqbhyrx in Phase 2-3 and pivotal studies; Phase 1b is a plus
• ability to manage complex design including SIVs and recruitment monitoring
• manage a substantial number of sites/subjects
• strong interpersonal and negotiation skills with investigators and site staff
• Spanish business level, English business level
• driven licence CRA
• willingness to grow scope of responsibilities

Requisitos principales
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📌 CRA (Madrid)
🏢 Les Laboratoires Servier
📍 Madrid