Senior Clinical Scientist
ICON is a integral healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Senior Clinical Scientist at ICON, you will design and conduct clinical studies that evaluate the safety and efficacy of innovative treatments.
What You Will Do:
- Contribute to the development and creation of clinical trial protocols following high scientific and clinical standards and applicable regulations.
- Contribute to the identification, formulation and implementation of amendments to the clinical protocol, in close collaboration with clinical lead.
- Contribute to the creation of study-level documents, including preparation of clinical sections of key regulatory documents, such as Investigator’s Brochures, briefing books, safety updates and submission dossiers.
- Contribute to the review and writing of clinical trial documents for CTR activities, and publications (as applicable)
- Support pharmacovigilance activities (e.g. contributing to creation and review of aggregate reports, patient narratives and attendance of pharmacovigilance monitoring meetings)
- Support regulatory activities (preparation of meetings with regulatory agencies).
- Produce training materials, share best practices and provide training to the broader clinical trial teams.
- Support preparation and (if applicable) participate in study level meetings (i.e. - Investigator Meetings, Data Monitoring meetings, and others).
- Support and guide the development of data review strategy, ensuring that protocol-level deviations, eligibility criteria, study assessments & other aspects of the protocol are implemented consistently across the study (across countries/ sites). Includes support for Case Report Form (CRF) development, and imple
📌 Senior Clinical Scientist (Madrid)
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📍 Madrid