Job DescriptionJob Responsibilities:1- Build and maintain good communication with central government stakeholders including National Healthcare Security Administration (NHSA) and related government agencies.2- Monitor the timeline principle and related policy of NRDL adjustment. Enlis
Job DescriptionJob Responsibilities:1- Build and maintain good communication with central government stakeholders including National Healthcare Security Administration (NHSA) and related government agencies.2- Monitor the timeline principle and related policy of NRDL adjustment. Enlis
Job DescriptionThe Director Training & Documentation provides strategic leadership for training documentation governance and process excellence within Safety Data Management (SDM). This role ensures global compliance inspection readiness and operational effectiveness across safety cas
Job DescriptionThe Director Training & Documentation provides strategic leadership for training documentation governance and process excellence within Safety Data Management (SDM). This role ensures global compliance inspection readiness and operational effectiveness across safety cas
Job DescriptionThe Technical PM is responsible for the end-to-end project management and delivery of technical deliverables for assigned clinical trials within a specific drug/vaccine program. Develops and manages technical project plans which span from design and specification develo
Job DescriptionThe Technical PM is responsible for the end-to-end project management and delivery of technical deliverables for assigned clinical trials within a specific drug/vaccine program. Develops and manages technical project plans which span from design and specification develo
Job DescriptionThe Specialist within Operational Enablement & Effectiveness (OEE) / MAP has experience in clinical operations and is responsible for the development of data analysis and visualizations in support of user needs across Global Clinical Trial Operations (GCTO) across our p
Job DescriptionThe Specialist within Operational Enablement & Effectiveness (OEE) / MAP has experience in clinical operations and is responsible for the development of data analysis and visualizations in support of user needs across Global Clinical Trial Operations (GCTO) across our p
Job DescriptionOur Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities along with our external contractors suppliers and partners create a reliable global manufacturing network that is devoted to delivering a
Job DescriptionOur Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities along with our external contractors suppliers and partners create a reliable global manufacturing network that is devoted to delivering a
Job DescriptionOur Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities along with our external contractors suppliers and partners create a reliable global manufacturing network that is devoted to delivering a
Job DescriptionOur Manufacturing & Supply Division is dedicated to being the most trusted supplier of biopharmaceuticals worldwide. Our facilities along with our external contractors suppliers and partners create a reliable global manufacturing network that is devoted to delivering a
Job DescriptionAbout the RoleJoin our HR Technology team as a Senior Specialist focused on supporting HR data privacy processes. You will support activities related to global data privacy requirements for HR systems and processes. You will support and consult across HR solutions to en
Job DescriptionAbout the RoleJoin our HR Technology team as a Senior Specialist focused on supporting HR data privacy processes. You will support activities related to global data privacy requirements for HR systems and processes. You will support and consult across HR solutions to en
Job DescriptionWe are seeking aQuality Assurance Specialistto join our quality team at the Carlow facility within theQuality Technical Transfer/Validation Team. This role will support theintroduction of new products (NPI)across our vaccine and biological manufacturing operations. It i
Job DescriptionWe are seeking aQuality Assurance Specialistto join our quality team at the Carlow facility within theQuality Technical Transfer/Validation Team. This role will support theintroduction of new products (NPI)across our vaccine and biological manufacturing operations. It i
Job DescriptionProvide overall business directions and leadership in a product franchise based on franchise goals. They are expected to develop marketing strategies for the product franchise team and ensure effective implementation of these strategies in the field. They should be the
Job DescriptionProvide overall business directions and leadership in a product franchise based on franchise goals. They are expected to develop marketing strategies for the product franchise team and ensure effective implementation of these strategies in the field. They should be the
Job DescriptionThe Sr Specialist within Operational Enablement & Effectiveness (OEE) / MAP has experience in clinical operations and is responsible for the development of data analysis and visualizations in support of user needs across Global Clinical Trial Operations (GCTO) across ou
Job DescriptionThe Sr Specialist within Operational Enablement & Effectiveness (OEE) / MAP has experience in clinical operations and is responsible for the development of data analysis and visualizations in support of user needs across Global Clinical Trial Operations (GCTO) across ou
Job DescriptionThe Sr Specialist within Operational Enablement & Effectiveness (OEE) / MAP has experience in clinical operations and is responsible for the development of data analysis and visualizations in support of user needs across Global Clinical Trial Operations (GCTO) across ou
Job DescriptionThe Sr Specialist within Operational Enablement & Effectiveness (OEE) / MAP has experience in clinical operations and is responsible for the development of data analysis and visualizations in support of user needs across Global Clinical Trial Operations (GCTO) across ou
Job DescriptionCOA Sr. Specialist is responsible for providing end-to-end COA systems project management support including but not limited to gathering study-specific user requirements executing UAT tasks managing project timelines managing and enforcing COA systems Standards. COA Sr.
Job DescriptionCOA Sr. Specialist is responsible for providing end-to-end COA systems project management support including but not limited to gathering study-specific user requirements executing UAT tasks managing project timelines managing and enforcing COA systems Standards. COA Sr.
Job DescriptionCOA Sr. Specialist is responsible for providing end-to-end COA systems project management support including but not limited to gathering study-specific user requirements executing UAT tasks managing project timelines managing and enforcing COA systems Standards. COA Sr.
Job DescriptionCOA Sr. Specialist is responsible for providing end-to-end COA systems project management support including but not limited to gathering study-specific user requirements executing UAT tasks managing project timelines managing and enforcing COA systems Standards. COA Sr.
Job DescriptionThis position leads the operational planning and execution of one or more clinical trials or significant aspects this position you will have the opportunity to demonstrate your leadership and technical skills as part of a global cross-functional team. You will apply pr
Job DescriptionThis position leads the operational planning and execution of one or more clinical trials or significant aspects this position you will have the opportunity to demonstrate your leadership and technical skills as part of a global cross-functional team. You will apply pr
Job DescriptionAt our company we aspire to be the premier research-intensive biopharmaceutical company using the power of leading-edge science to save and improve lives around the world. We are at the forefront of research to deliver innovative health solutions that advance the preven
Job DescriptionAt our company we aspire to be the premier research-intensive biopharmaceutical company using the power of leading-edge science to save and improve lives around the world. We are at the forefront of research to deliver innovative health solutions that advance the preven
Job DescriptionThis role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the CRD or Head of Site Management and Monitoring the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adhe
Job DescriptionThis role will be key to ensure strong monitoring in our clinical trials. Under the oversight of the CRD or Head of Site Management and Monitoring the person is responsible to manage a team of 6-14 CRAs and to ensure excellent study and site performance with strict adhe
Job DescriptionThe company Device Product and Process Development (DPPD) Team is seeking a hands-on device characterization and design focused technical leader. This position will be responsible for technical interrogation of the various drug delivery device technology platforms suppo
Job DescriptionThe company Device Product and Process Development (DPPD) Team is seeking a hands-on device characterization and design focused technical leader. This position will be responsible for technical interrogation of the various drug delivery device technology platforms suppo
Job DescriptionWe are seeking a highly motivated collaborative and outcomes-driven leader to join our companys Digital Human Health (DHH) organization and play an active role in our companys Human Health transformation journey to become the premier Data First commercial biopharma orga
Job DescriptionWe are seeking a highly motivated collaborative and outcomes-driven leader to join our companys Digital Human Health (DHH) organization and play an active role in our companys Human Health transformation journey to become the premier Data First commercial biopharma orga
Job DescriptionThis Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations guidances and defined regulatory strategies as well as the preparation and review of information required for development of re
Job DescriptionThis Role is responsible for implementing CMC regulatory strategies for assigned pharmaceutical products in accordance with global regulations guidances and defined regulatory strategies as well as the preparation and review of information required for development of re
Job DescriptionJob PostingPrivacy Steward and Business Practices / Compliance SpecialistIntroductionJoin our companys Business Practices Compliance team in Belgium in a role that combines privacy responsibilities with broader business practices and compliance activities.In this role y
Job DescriptionJob PostingPrivacy Steward and Business Practices / Compliance SpecialistIntroductionJoin our companys Business Practices Compliance team in Belgium in a role that combines privacy responsibilities with broader business practices and compliance activities.In this role y