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The Associate Director, Global Oncology HEOR & RWE will work cross-functionally to implement HEOR and RWE projects for the assigned assets under the direction of a Director or Sr. Director of Global Oncology HEOR & RWE. The person will work with clinical, market access, commercial, regional and medical affairs colleagues to support the clinical development and value creation of the company's oncology assets.
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Key partnerships include Commercial, Real-World Evidence, Commercial Analytics, Medical Affairs and Market Access as well as outside GCSO with regional Commercial and Medical/Scientific Affairs teams, J&JIM R&D, J&J Technology (JJT) Data Sciences and broader J&JIM teams, and others.
$142,000 - $244,950 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Director, Global Commercial Digital Health, will lead the strategy development and commercialization of digital health solutions globally and build industry-leading Digital Health capabilities in Global Commercial Data Science (GCDS) and across the J&JIM GCSO in support of our therapeutic areas and disease area strongholds globally.
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In collaboration with medical director, Digital Medicine Lead, QS, and others, design study; execute on sensor-facing aspects of CES study, including liaison with vendor/device collaborator and User Experience Research (UXR.
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With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000 employees around the world draw upon a rich legacy of innovation and a robust pipeline of promising new medicines to help people.
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The Director collaborates with key stakeholders across the company including Training/Medical Excellence, Field-based/ Medical Outcomes Liaisons (MOLs)/Medical Science Liaison (MSL), market access, payer marketing, global medical strategy, and other HEOR team members, to support Insmeds business needs.
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Ensure HEOR communication tools (e.g. medical/payer presentation decks for internal and external use, value dossiers, interactive economic models, publications, and other reactive and proactive evidence content for external stakeholders) are strategic, impactful, and aligned with crosstunctional team needs; working in close partnership with other HEOR team members, publication/ scientific communications, global medical strategy and market access.
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Leads external medical education and other scientific exchange activities in alignment with the Senior Director, such as scientific symposium and medical congresses, within legal and compliance regulations.
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The purpose of this job is to provide statistical programming technical support to DSI project teams on all statistical programming deliverables and programming submission. Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology.
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This position reports to VP, CDMA with a dotted line reporting relationship to the CSO. The Senior Director CDMA will interact with internal colleagues in Research and Development (Clinical Development & Medical Affairs, Strategic Operations, Evidence Generation & Data Sciences, Regulatory Affairs, Pharmacovigilance) Strategy/Portfolio Management,Commercial and Operations functions.
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Contributes to the scientific literature in the form of manuscripts and publications. Presents at professional scientific meetings teach courses, collaborates with external investigators, and communicates with scientific personnel at regulatory agencies.
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BS/BA degree in a relevant scientific discipline or MSc in Biology, Life Science, or related field with at least 5 years of relevant pharmaceutical/biotechnology industry experience, including at least 3 years of relevant Regulatory Affairs experience, or Advanced degree (PharmD, PhD, MD or DVM) with at least 2 years of regulatory or relevant pharmaceutical/biotechnology industry experience required.
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Collaborates across GMA functions to develop, review, and align on key scientific communications and medical information response documents within legal and compliance regulations. Provides medical leadership in scientific engagement activities with key external stakeholders such as advisory boards, investigator interactions, congress activities, peer to peer discussions with key thought leaders.
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Advanced degree in a scientific discipline: MD, PhD, PharmD. Lead medical and scientific advisory boards to capture insights and translate into medical strategy. Provide inspirational leadership to the US Medical Affairs Immunology (Non-Alliance) team (Medical Directors, Medical Science Liaison Managers, MSLs) by cultivating a culture of teamwork and collaboration to ensure the delivery of key priorities, while attracting, developing and retaining top talent.
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The Medical Science Liaison (MSL) develops and maintains professional relationships with external healthcare practitioners to provide comprehensive medical and scientific support for Insmed assigned therapeutic areas.
$200,000 - $260,000 a yearFull-timeExpandApply NowActive JobUpdated 27 days ago
scientific director jobs in Bridgewater, NJ
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