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designed to prepare post-doctoral scholars for rewarding careers in the biopharmaceutical industry. Through hands-on experience, Fellows will work with various cross-functional teams to learn the role
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, and infographics for external healthcare providers. Provide medical review of scientific engagement material (non-promotional) and commercial (promotional) material Develop pre- and post-authorization
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approach to channel strategy across the value chain, ensuring reliable product access and distribution across the portfolio. This will include helping prepare for launches and post-approval pull-through by
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activities, including medical booth planning and staffing, scientific communication and engagement activities, and participation in internal post-congress debriefs. Cross-Functional Collaboration and
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and coordinating regulatory submissions necessary to support clinical trials, product registrations, post marketing requirements and commitments, and product-claim promotional materials SUPPORT
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) Global HEOR activities In support of US launch – pre-approval information exchange (PIE) tools and post-approval value tools Strategy and planning related to various country-specific health authority (HTA
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Responsibilities: · Assist in the planning and coordinating all aspects of regulatory submissions necessary to support clinical trials, product registrations, and post marketing requirements and commitments