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years in safety at an operational or medical position • Experience in preparing or contributing to preparation of clinical safety assessments and regulatory re- ports/submissions involving safety
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information from all sources through lifecycle management. This role will work directly with the Medical Safety Development team and reports to the Head Patient Safety CRM. Key Responsibilities: • Providing
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); ensuring that this team reviews all medical safety data from various sources (e.g. pre-clinical, clinical trial data post-marketing, literature) throughout the development and post-approval process in
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