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            "description": "<p>Associate Director, Clinical Database Applications and Reporting at Daiichi Sankyo Company,Limited - Job Location (Country/Region) - Associate Director, Clinical Database Applications and Reporting Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to &quot;be an innovative global healthcare company contributing to the sustainable development of society&quot;, we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary Summary The Associate Director, Clinical Database Applications and Reporting is a member of the Biostatistics and Data Management team and serves as a subject matter expert responsible for setting the overall programming strategy including the oversight, guidance, implementation, and management of clinical database applications and reporting. The responsibilities include advancing operational excellence by standardizing reporting, scaling programming strategies, automating workflows, and delivering high-quality outputs that meet user requirements by collaborating with variety of internal and external stakeholders including leading all aspects of end-to-end programming efforts. In addition managing quality of data validation programming deliverables; maintaining compliance and inspection readiness of clinical applications, reports, and supporting process documentation; and reporting process are some of the key re</p>",
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            "description": "<p>Senior Manager (m/w/d) Production Excellence &amp; Operational Support at Daiichi Sankyo Company,Limited - Job Location (Country/Region) - Senior Manager (m/w/d) Production Excellence &amp; Operational Support Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to &quot;be an innovative global healthcare company contributing to the sustainable development of society&quot;, we are shaping a healthier, more hopeful future for patients, their families, and society. Die Position: Verantwortlich fuer die Steuerung und Weiterentwicklung von Validierungs- und Qualifizierungsstrategien im Produktionsumfeld, die uebergreifende Unterstuetzung der Betriebsabteilungen sowie die Fuehrung komplexer, bereichsuebergreifender GMP-Themen und Projekte mit massgeblichem Einfluss auf Compliance, Inspektionsfaehigkeit und die nachhaltige Optimierung von Produktionsstandards. Angaben zur Tätigkeit: Selbstständige Planung, Steuerung und Verantwortung von komplexen Validierungsprojekten im Produktionsumfeld (Herstell- und Reinigungsprozesse sowie aseptische Produktionsverfahren) Gesamtverantwortung für Qualifizierungsstrategien (PQs) und deren Umsetzung Konzeptionelle Mitgestaltung von Anlagen, Technologien und Investitionen Selbstständige Vertretung der Produktion bei Produkttransfers im Rahmen von Site-Launch-Teams Verantwortung für die Bearbeitung komplexer Abweichungen inkl. systemischer Ursachenanalys</p>",
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            "description": "<p>Werkstudent Quality Operations (m/w/d) - Bereich Packaging at Daiichi Sankyo Company,Limited - Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region) - Werkstudent Quality Operations (m/w/d) - Bereich Packaging Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to &quot;be an innovative global healthcare company contributing to the sustainable development of society&quot;, we are shaping a healthier, more hopeful future for patients, their families, and society. Die Position: Wir suchen ab sofort für unseren Entwicklungs- und Produktionsstandort in Pfaffenhofen/Ilm eine/n engagierte/n Werkstudent Quality Operations (m/w/d) - Bereich Packaging Sie unterstützen dabei unsere QA-Administrator/-innen vor Ort in der Verpackung bei ihren Routinetätigkeiten zur Kontrolle und Verwaltung der QA-seitigen Überwachung der Verpackungsdokumentation. Angaben zur Tätigkeit: Schwerpunkt: Organisation und Durchführung der Ablage und Archivierung der fertigen, abgeschlossenen Chargendokumentationen in der Verpackung. Unterstützung der QA-Administrator/-innen beim Batch Record Review durch Zusammenstellung von Dokumentationen. Ggf. Unterstützung der QA-Administratorinnen beim Ausgabereview in der Verpackung. Kontrollierte Ausgabe und Verwaltung von Formularen in der Verpackung. Unterstützung des Vorgesetzten für QA-relevante Tätigkeiten bei Bedarf. Fachliche und persönliche Anforderungen: Universitäts-</p>",
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            "title": "Senior Manager, Clinical Database Applications and Reporting (m/f/d)",
            "description": "<p>Senior Manager, Clinical Database Applications and Reporting (m/f/d) at Daiichi Sankyo Company,Limited - Job Location (Country/Region) - Senior Manager, Clinical Database Applications and Reporting (m/f/d) Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to &quot;be an innovative global healthcare company contributing to the sustainable development of society&quot;, we are shaping a healthier, more hopeful future for patients, their families, and society. The Position The Associate Director, Clinical Database Applications and Reporting is a member of the Biostatistics and Data Management team and serves as a subject matter expert responsible for setting the overall programming strategy including the oversight, guidance, implementation, and management of clinical database applications and reporting. The responsibilities include advancing operational excellence by standardizing reporting, scaling programming strategies, automating workflows, and delivering high-quality outputs that meet user requirements by collaborating with a variety of internal and external stakeholders including leading all aspects of end-to-end programming efforts. In addition, managing quality of data validation programming deliverables, maintaining compliance and inspection readiness of clinical applications, reports, and supporting process documentation, and reporting processes are some of the key requ</p>",
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            "description": "<p>Senior Manager (m/w/d) Audit &amp; Supplier Qualification at Daiichi Sankyo Company,Limited - Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region) - Senior Manager (m/w/d) Audit &amp; Supplier Qualification Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to &quot;be an innovative global healthcare company contributing to the sustainable development of society&quot;, we are shaping a healthier, more hopeful future for patients, their families, and society. Purpose of the function For our Daiichi Sankyo Europe GmbH headquarters in Munich we are currently seeking highly qualified candidates to fill the position: Senior Manager (m/f/d) Audit &amp; Supplier Qualification Roles and Responsibilities Audit Planning &amp; Execution: Plan and perform GMP/GDP Audits at Contract Manufacturing Organizations (CMOs) or Suppliers Prepare audit findings &amp; reports and discuss potential impact on business Responsible for Follow-Up communication related to audits with CMOs &amp; Suppliers and monitor CAPA implementation related to audit findings Internal consultation for risk identification with day-to-day business &amp; QA functions related to CMOs/Suppliers Quality Agreements: Support global and regional Quality Agreement template definition Negotiate Quality Agreements with CMOs and Suppliers Involve internal stakeholders in Quality Agreement negotiations whenever required Support Integrated Risk Management</p>",
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            "title": "Medical Science Liaison, GYN Oncology - West",
            "description": "<p>Medical Science Liaison, GYN Oncology - West at Daiichi Sankyo Company,Limited - Work Model Remote (Daiichi Sankyo US) | Job Location (Country/Region) - Medical Science Liaison, GYN Oncology - West Work Model Remote (Daiichi Sankyo US) | Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to &quot;be an innovative global healthcare company contributing to the sustainable development of society&quot;, we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary The Medical Science Liaison develops ongoing professional relationships with national and regional healthcare opinion leaders and other healthcare professionals to provide medical and scientific support for Daiichi Sankyo, Inc. (DSI) initiatives in selected therapeutic areas. The MSL develops skills and competencies to educate healthcare professionals, DSI internal stakeholders (e.g., Medical, Marketing, and Sales), and decision makers in healthcare systems regarding therapeutic areas and related products developed and commercialized by DSI. This is a US Medical Affairs, Field based role. This territory currently covers the following states: AK, WA, OR, CA, AZ, NV, UT, ID, MT, Northern and West WY. Responsibilities Builds and maintains professional relationships with healthcare professionals (HCPs) by developing the skills and with guidance, implementing the following: Presenting disease state and Daiichi Sankyo</p>",
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            "description": "<p>Working Student (m/f/d) Global Oncology Pricing Analytics, Operations &amp; Payer Excellence at Daiichi Sankyo Company,Limited - Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region) - Working Student (m/f/d) Global Oncology Pricing Analytics, Operations &amp; Payer Excellence Work Model Office Based Role (Daiichi Sankyo Europe) | Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to &quot;be an innovative global healthcare company contributing to the sustainable development of society&quot;, we are shaping a healthier, more hopeful future for patients, their families, and society. Purpose of the function We are currently seeking a Working Student to join our Global Oncology Value, Access and Pricing (GOVAP) team in our European headquarters in Munich. In this role, you will support the GOVAP Pricing Analytics, Operations and Payer Excellence team in executing pricing activities that contribute to the development of market access strategies across Daiichi Sankyo&#39;s portfolio. Roles and Responsibilities Support internal pricing governance processes by ensuring that business cases and approvals for pricing decisions are appropriately reviewed and documented. Support with management of Daiichi Sankyo&#39;s internal pricing approval platform: maintaining system accuracy through data quality checks, acting as a main contact for user guidance and onboarding, and coordinating the resolution of any technical issues that arise in the platform. Support with the development of pricing approval platform enhancements b</p>",
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            "description": "<p>Sr Analyst Engagement Monitoring at Daiichi Sankyo Company,Limited - Job Location (Country/Region) - Sr Analyst Engagement Monitoring Job Location (Country/Region) At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to &quot;be an innovative global healthcare company contributing to the sustainable development of society&quot;, we are shaping a healthier, more hopeful future for patients, their families, and society. Job Summary This position is primarily responsible for monitoring / auditing HCP (Health Care Provider) activities for all engagements pertaining to their travel and/or attendance at meetings, speaker programs, and conventions as well as single engagements in support of DSI (commercial and development organizations). This role is also responsible for monitoring and auditing all non-HCP meetings and activities according to DSI policies. The role will have primary responsibility within Corporate Programs &amp; Events for ensuring DSI&#39;s compliance with all CIA related policies, state and federal regulations regarding payments to HCPs and reporting of such for the listed activities. Job Description Responsibilities HCP Engagement folders - Establish and manage the monthly HCP Engagement Folder audit process, to ensure information is documented and reported timely. Folder Audit includes: Review HCP Engagements that are considered cl</p>",
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