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with brand strategies to support successful pre-launch, launch, post-launch medical initiatives. ROLE RESPONSIBILITIES Product Strategy and Brand Plan Development: Oversee and coordinate medical input
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Affairs is preferred Experience in Gastroenterology is preferred NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS Ability to travel up to 25% in post-pandemic timeframe Other Job Details: Last
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engineering controls and target product attributes are met . Support data review and present learnings post- manufactu re . D rive the timely resolution of quality deviations and assist in root cause analysis
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, e.g., GDMS. Finalize documents post QC (including update of GDMS document properties such as entry of PfLEET2 number, update of document title, update CDS cover page etc.). Manage the document status in
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the development and post-approval environment through consultation and implementation of statistical techniques related to HEOR based on state-of-the-art research. Enhance statistical expertise in value-based drug
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around labeling and associated supportive documentation, both in the pre-approval and post approval (maintenance) stages. Demonstrated ability to develop strong and positive working relationships across