Cordula Landgraf
Director Communications & Stakeholder Engagement; Deputy Managing Director at Swiss Clinical Trial Organisation- Claim this Profile
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French Professional working proficiency
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English Full professional proficiency
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German Native or bilingual proficiency
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Bio
Bruno Gander
Cordula Landgraf has been a guest lecturer in Regulatory Affairs in the MSc Pharmaceutical Sciences program (formerly Medicinal and Industrial Pharmaceutical Sciences, MIPS) at the ETH Zurich since 2008. Her most competent and didactically skillful teaching has been greatly appreciated by students, colleague lecturers, the director of studies, and by myself in my function as study program coordinator. On a personal level, she is very empathetic, warmhearted, thoughtful, and full of fine humor.
Andreas Balsiger Betts
Cordula Landgraf is a professional in the best sense of the term. She is highly qualified with regard to regulatory science in the pharmaceutical sector (globally, but with special emphasis on Europe and Switzerland). She has a wide network within the regulatory community, is an excellent speaker (both in German and English) and represents very well. Last but not least it is a pleasure to work with her, both on a daily basis as a colleague but also in projects and in conference work; she is diligent, friendly and fun to be with.
Bruno Gander
Cordula Landgraf has been a guest lecturer in Regulatory Affairs in the MSc Pharmaceutical Sciences program (formerly Medicinal and Industrial Pharmaceutical Sciences, MIPS) at the ETH Zurich since 2008. Her most competent and didactically skillful teaching has been greatly appreciated by students, colleague lecturers, the director of studies, and by myself in my function as study program coordinator. On a personal level, she is very empathetic, warmhearted, thoughtful, and full of fine humor.
Andreas Balsiger Betts
Cordula Landgraf is a professional in the best sense of the term. She is highly qualified with regard to regulatory science in the pharmaceutical sector (globally, but with special emphasis on Europe and Switzerland). She has a wide network within the regulatory community, is an excellent speaker (both in German and English) and represents very well. Last but not least it is a pleasure to work with her, both on a daily basis as a colleague but also in projects and in conference work; she is diligent, friendly and fun to be with.
Bruno Gander
Cordula Landgraf has been a guest lecturer in Regulatory Affairs in the MSc Pharmaceutical Sciences program (formerly Medicinal and Industrial Pharmaceutical Sciences, MIPS) at the ETH Zurich since 2008. Her most competent and didactically skillful teaching has been greatly appreciated by students, colleague lecturers, the director of studies, and by myself in my function as study program coordinator. On a personal level, she is very empathetic, warmhearted, thoughtful, and full of fine humor.
Andreas Balsiger Betts
Cordula Landgraf is a professional in the best sense of the term. She is highly qualified with regard to regulatory science in the pharmaceutical sector (globally, but with special emphasis on Europe and Switzerland). She has a wide network within the regulatory community, is an excellent speaker (both in German and English) and represents very well. Last but not least it is a pleasure to work with her, both on a daily basis as a colleague but also in projects and in conference work; she is diligent, friendly and fun to be with.
Bruno Gander
Cordula Landgraf has been a guest lecturer in Regulatory Affairs in the MSc Pharmaceutical Sciences program (formerly Medicinal and Industrial Pharmaceutical Sciences, MIPS) at the ETH Zurich since 2008. Her most competent and didactically skillful teaching has been greatly appreciated by students, colleague lecturers, the director of studies, and by myself in my function as study program coordinator. On a personal level, she is very empathetic, warmhearted, thoughtful, and full of fine humor.
Andreas Balsiger Betts
Cordula Landgraf is a professional in the best sense of the term. She is highly qualified with regard to regulatory science in the pharmaceutical sector (globally, but with special emphasis on Europe and Switzerland). She has a wide network within the regulatory community, is an excellent speaker (both in German and English) and represents very well. Last but not least it is a pleasure to work with her, both on a daily basis as a colleague but also in projects and in conference work; she is diligent, friendly and fun to be with.
Credentials
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Strategic Thinking
LinkedInJul, 2022- Sep, 2024 -
Executive Presence on Video Conference Calls
LinkedInNov, 2020- Sep, 2024 -
Gehirngerechtes Lernen
LinkedInSep, 2019- Sep, 2024
Experience
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Swiss Clinical Trial Organisation
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Switzerland
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Research Services
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1 - 100 Employee
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Director Communications & Stakeholder Engagement; Deputy Managing Director
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Jun 2020 - Present
- Leading and directing the Communication & Stakeholder Engagement team - Further developing SCTO's communication concept - Strategic stakeholder engagement/management with special focus on patient involvement - "Ambassador" for the SCTO - Representing the SCTO in national/international committees, working groups, etc. - Issue and knowledge management - Event management - Speaker/lecturer at internal and external events - Leading and directing the Communication & Stakeholder Engagement team - Further developing SCTO's communication concept - Strategic stakeholder engagement/management with special focus on patient involvement - "Ambassador" for the SCTO - Representing the SCTO in national/international committees, working groups, etc. - Issue and knowledge management - Event management - Speaker/lecturer at internal and external events
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IFAPP - International Federation of Associations of Pharmaceutical Physicians & Pharm. Medicine
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Netherlands
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Member of the IFAPP Board, Standing Officer and Chair of the External Affairs Working Group
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Jun 2021 - Present
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EUPATI Switzerland/ Schweiz / Suisse / Svizzera (EUPATI CH)
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Switzerland
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Non-profit Organizations
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Member of the EUPATI CH Executive Board
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Apr 2021 - Present
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SFL Regulatory Affairs & Scientific Communication GmbH
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Switzerland
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Biotechnology Research
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1 - 100 Employee
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Head Public Affairs & Regulatory Policy
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Oct 2019 - Mar 2020
- Leading the SFL Public Affairs & Regulatory Policy team - Oversight of SFL external communication - Oversight of client projects in the areas of public affairs, association management and regulatory intelligence - Representation of SFL in trade association EuropaBio and at international meetings - Analysis and impact assessment of EU and Swiss legislative/policy developments - Issue Management - Project lead for Medtech & Pharma Platform (MPP) Annual Conference 2020 - Leading the SFL Public Affairs & Regulatory Policy team - Oversight of SFL external communication - Oversight of client projects in the areas of public affairs, association management and regulatory intelligence - Representation of SFL in trade association EuropaBio and at international meetings - Analysis and impact assessment of EU and Swiss legislative/policy developments - Issue Management - Project lead for Medtech & Pharma Platform (MPP) Annual Conference 2020
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Head of Networking
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Aug 2007 - Sep 2019
Responsible for the coordination of national and international co-operation with stakeholders - Stakeholder engagement - Policy and strategic concept development - Member of the ICH Management Committee and Assembly - Member of the EUPATI Regulatory Advisory Panel - Chair of the Swissmedic Working Group with patients' and consumer organisations - Lecturer at Master curriculum Pharmaceutical Sciences at ETH Zurich/Switzerland - Lecturer at MEGRA StartUp CH training course and honorary member of MEGRA (Mitteleuropäische Gesellschaft für Regulatory Affairs) - Member of DGRA (Deutsche Gesellschaft für Regulatory Affairs) and lecturer at MDRA study course - Member of DIA’s Regional Advisory Council Europe, Middle East & Asia Show less
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ALTANA Pharma AG
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Pharmaceutical Manufacturing
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1 - 100 Employee
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Regulatory Intelligence Manager
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Aug 2003 - Jun 2007
- Monitoring and assessing the international regulatory environment including authority decisions and competitor information - Active contribution to developmental Regulatory Affairs work from early development on - Participating at strategic regulatory decision-making - Training Regulatory Affairs staff on regulatory requirements / new developments - Monitoring and assessing the international regulatory environment including authority decisions and competitor information - Active contribution to developmental Regulatory Affairs work from early development on - Participating at strategic regulatory decision-making - Training Regulatory Affairs staff on regulatory requirements / new developments
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Senior Regulatory Affairs Associate
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Oct 2001 - Jul 2003
- Preparation and submission of variations and renewal applications - Compilation and submission of registration dossiers for NCEs - Preparation and filing of answers to Regulatory Authorities' deficiency letters - Preparation of Pre-filing / Scientific Advice meetings - Liaison with Regulatory Authorities (international) - Preparation and submission of variations and renewal applications - Compilation and submission of registration dossiers for NCEs - Preparation and filing of answers to Regulatory Authorities' deficiency letters - Preparation of Pre-filing / Scientific Advice meetings - Liaison with Regulatory Authorities (international)
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Education
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1989 - 1995
Johann Wolfgang Goethe-Universität Frankfurt am Main
Staatsexamen, Pharmazie
Community
