Director of Regulatory Affairs and Clinical Trials

Director of Regulatory Affairs and Clinical Trials (m/f/x), Regulatory Affairs EuropePosition Overview:This Senior Director role is designed to deliver regulatory expertise, strategic guidance, and project oversight for designated initiatives, ensuring alignment with scientific integrity and commercial feasibility while adhering to regulatory requirements....

Director of Regulatory Affairs and Clinical Trials (m/f/x), Regulatory Affairs EuropePosition Overview:This Senior Director role is pivotal in delivering regulatory expertise, strategic direction, and project oversight to designated initiatives, ensuring alignment with scientific integrity and commercial viability while adhering to regulatory frameworks. Key...

Position Overview:The Senior Director of Regulatory Affairs and Clinical Trials will spearhead regulatory strategy, oversight, and project management to ensure compliance with industry standards while driving scientific and commercial success. This role encompasses leading the Regulatory Procedures and Project Management team, offering managerial guidance to...

Position Overview:The Senior Director role is pivotal in steering regulatory initiatives, offering strategic guidance, and managing projects with a focus on procedural excellence within the realm of clinical trials. This position demands a comprehensive understanding of regulatory frameworks and a commitment to maintaining high standards of compliance.Key...

About the Role:We are seeking a highly qualified Director of Global Regulatory Affairs to join our team at Daiichi Sankyo Europe GmbH. As a key member of our global product team, you will be responsible for providing European regulatory strategy support for assigned projects, products, and non-project work.Key Responsibilities:Provide European regulatory...

About the Role:We are seeking a highly qualified Director of Global Regulatory Affairs to join our team at Daiichi Sankyo Europe GmbH. As a key member of our global product team, you will be responsible for providing European regulatory strategy support for assigned projects, products, and non-project work.Key Responsibilities:Provide European regulatory...

About Daiichi Sankyo EuropeDaiichi Sankyo Europe is a leading pharmaceutical company dedicated to discovering, developing, and delivering innovative treatments that enrich the quality of life for patients worldwide.Our MissionWe strive to become a global pharma innovator with a competitive advantage, creating novel therapies for people with cancer and...

About Daiichi Sankyo EuropeDaiichi Sankyo Europe is a leading pharmaceutical company dedicated to discovering, developing, and delivering innovative treatments that enrich the quality of life for patients worldwide.Our MissionWe strive to become a global pharma innovator with a competitive advantage, creating novel therapies for people with cancer and...

About Daiichi Sankyo Europe GmbHDaiichi Sankyo Europe GmbH is a leading pharmaceutical company dedicated to discovering, developing, and delivering innovative treatments that improve the quality of life for patients worldwide.Our MissionWe strive to become a global pharma innovator with a competitive advantage, creating novel therapies for people with...

About Daiichi Sankyo Europe GmbHDaiichi Sankyo Europe GmbH is a leading pharmaceutical company dedicated to discovering, developing, and delivering innovative treatments that improve the quality of life for patients worldwide.Our MissionWe strive to become a global pharma innovator with a competitive advantage, creating novel therapies for people with...

Your RoleEngage in intricate product development projects alongside R&D and project management teams, identifying potential clinically significant issues arising from feature deficiencies and their clinical implications. Formulate and execute the necessary clinical evaluation strategies and clinical studies for the product.Oversee budget and timeline...

About Novotech Clinical Research GmbHWe are a global full-service clinical Contract Research Organization (CRO) focused on partnering with biotech companies to accelerate the development of advanced and novel therapeutics at every phase.Our ExpertiseWe offer a comprehensive suite of services including:Regulatory Expertise: Ensuring compliance with regulatory...

About the RoleWe are seeking a highly skilled Clinical Trials Manager to join our team at EPM Scientific. As a key member of our clinical development team, you will be responsible for the management and coordination of clinical trials in the Neurology field.Key ResponsibilitiesManage and coordinate clinical trials from planning to completionDevelop and...

About the RoleWe are seeking a highly skilled Clinical Trials Manager to join our team at EPM Scientific. As a key member of our clinical development team, you will be responsible for the management and coordination of clinical trials in the Neurology field.Key ResponsibilitiesManage and coordinate clinical trials from planning to completionDevelop and...

Job SummaryAspire Life Sciences Search is seeking a highly experienced and skilled Director of Regulatory and Quality Affairs to lead our client's regulatory and quality initiatives across all product lines. This is a critical role that will play a key part in ensuring compliance with both EU and US regulatory requirements, overseeing product registrations,...

Job SummaryAspire Life Sciences Search is seeking a highly experienced and skilled Director of Regulatory and Quality Affairs to lead our client's regulatory and quality initiatives across all product lines. This is a critical role that will play a key part in ensuring compliance with both EU and US regulatory requirements, overseeing product registrations,...

Junior Project Manager in Clinical Research (Oncology)Location: Germany (Candidates can be located anywhere in Germany. Please note that relocation or sponsorship cannot be provided for this role).About ScientaScienta is a pioneering organization in the field of oncology research, committed to advancing innovative treatments and transforming cancer care. As...

About the RoleWe are seeking a highly experienced and skilled Senior Regulatory Affairs Manager to join our team at Innovaderm Research. As a key member of our Regulatory Affairs department, you will be responsible for leading and managing regulatory activities across various regions, ensuring compliance with applicable regulations and good clinical...

About the RoleWe are seeking a highly experienced and skilled Senior Regulatory Affairs Manager to join our team at Innovaderm Research. As a key member of our Regulatory Affairs department, you will be responsible for leading and managing regulatory activities across various regions, ensuring compliance with applicable regulations and good clinical...

About the RoleWe are seeking a highly experienced and skilled Senior Regulatory Affairs Manager to join our team at Innovaderm Research. As a key member of our Regulatory Affairs department, you will be responsible for leading and managing regulatory activities across various regions, ensuring compliance with applicable regulations and good clinical...