Experteer Overview

Aunque la experiencia profesional y las cualificaciones son clave para este puesto, asegúrese de comprobar si posee las habilidades interpersonales preferibles antes de solicitar, si se requieren.
In this role you design and conduct clinical studies to assess safety and efficacy of innovative therapies. You work within the clinical development team to shape protocols, study documents, and data strategies, ensuring scientific rigour and regulatory alignment. You will drive data review and insights across the study lifecycle, support pharmacovigilance and regulatory activities, and help train and enable trial teams. This position offers impact across integral studies with a patient-focused mission and opportunities to improve trial quality and safety.

Compensaciones / Beneficios
• Design and conduct clinical studies and develop protocols to high scientific and regulatory standards
• Draft amendments to protocols in collaboration with the clinical lead
• Create study-level documents and regulatory submissions such as Investigator's Brochures and safety updates
• Review and write clinical trial documents for CTR activities and publications
• Support pharmacovigilance activities, including aggregate reports and patient narratives
• Assist regulatory activities and preparation for meetings with agencies
• Produce training materials and train trial teams




• Participate in study-level meetings and data review governance
• Develop data review strategy to ensure protocol adherence and consistent implementation across sites
• Perform in-depth clinical data review, identify insights, and support interim analyses and post-lock activities
• Improve quality of data reviews and implement data analytics enhancements
• Collaborate closely with the clinical development lead to address medical oversight questions

Responsabilidades
• Advanced degree in life sciences/healthcare or clinically relevant degree
• Minimum 5+ years' experience as a Clinical Scientist
• Oncology experience is a big xqbhyrx plus
• Knowledge of global clinical study setup, organization and execution in pharma or CRO
• Strong understanding of clinical data collection and reporting; proficient with data tools (e.g., EDC, Excel)
• Ability to drive process and tool improvements
• Experience working in a matrix environment with informal influencing ability
• Home Based with no travel

Requisitos principales
• Annual leave entitlements
• Health insurance offerings
• Competitive retirement planning
• Global Employee Assistance Programme, LifeWorks
• Life assurance
• Flexible country-specific optional benefits

📌 Senior Clinical Scientist (Madrid)
🏢 Icon Clinical
📍 Madrid