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for this role include executing core MI science-related activities for a designated portfolio by leveraging expertise with MI science skills in ensuring the delivery of high quality medical and scientific
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lead dashboard design Collaborate with Medical Impact and Outcomes team lead to ensure KPIs can be visualized in easy to read and understand dashboards Lead "user research" with MCCDH Planning and Impact
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Activation Partner, CTRO and Local Regulatory, Medical Affairs colleagues and other key stakeholders as required) Ensures compliance to relevant Global and Local, internal and external requirements and
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documents Facilitate team and cross functional meetings. Education Qualifications: Bachelor's degree in a science or life sciences required 3+ years experience in a regulated environment; pharmaceutical
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labeling experience preferred). Bachelor's degree (in science or life sciences preferred) Attributes: Knowledge of global/regional regulatory guidelines and requirements important. Excellent written and