Lecturer in Global Affairs

Director of Medical Affairs - AmericasAbbott Laboratories stands as a prominent global healthcare innovator dedicated to enhancing lives across all phases of existence. Our extensive range of transformative technologies encompasses various healthcare sectors, featuring leading businesses and products in diagnostics, medical devices, nutritionals, and branded...

Director of Medical Affairs - AmericasAbbott Laboratories stands as a prominent figure in the global healthcare landscape, dedicated to enhancing the quality of life across various stages. Our extensive portfolio encompasses innovative technologies that span diagnostics, medical devices, nutrition, and branded generic medicines, with a workforce of 114,000...

Director of Medical Affairs - AmericasAbbott Laboratories stands as a premier entity in the healthcare sector, dedicated to enhancing the quality of life for individuals across various stages. Our extensive portfolio encompasses transformative technologies across diagnostics, medical devices, nutrition, and branded generic medications. With a workforce of...

About the RoleWe are seeking a highly skilled Senior Manager, Regulatory Affairs to join our team at Sun Pharmaceutical Industries, Inc. This is a critical role that will play a key part in ensuring the success of our regulatory affairs function.Key ResponsibilitiesManage and coordinate global regulatory submission activities, ensuring timely and accurate...

Job SummaryTaiho Oncology, Inc. is seeking a highly skilled Regulatory Affairs Operations Director to join our team. As a key member of our Regulatory Affairs department, you will be responsible for managing global regulatory operational activities for all Taiho Oncology, Inc. projects.Key ResponsibilitiesRegulatory Operations Management: Manage global...

About the RoleGenmab A/S is seeking a highly skilled Director/Associate Director to join our Regulatory Affairs CMC team. As a key member of our team, you will be responsible for developing and executing global regulatory CMC strategies for biological products during early and late-stage development, and lifecycle.Key ResponsibilitiesDevelop and execute...

Senior Director, Global Regulatory Affairs StrategyThe position will provide regulatory affairs strategic leadership for Sun Pharmaceutical Industries, Inc. and novel drug development programs. Of each program this position supports, the individual will be responsible for developing and executing the overall regulatory strategy, which includes developing the...

Job SummaryThe Director, Global Regulatory Lead will be responsible for leading the development and execution of regulatory strategies for assigned brand programs. This role will provide strategic, tactical, and operational direction and guidance for product's pipeline and key regulatory milestones.Key ResponsibilitiesServe as key corporate regulatory...

About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting data to support efficacy and new product...

Position OverviewOur esteemed client in the pharmaceutical sector is in search of a Director of Regulatory Affairs for Chemistry Manufacturing & Controls (CMC). This role is pivotal in steering global teams through the intricacies of regulatory strategy and the formulation of CMC elements within drug development initiatives. Collaboration with various...

Job SummaryClinical Resource Network (CRN) is seeking a highly skilled CMC Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs department, you will be responsible for providing strategic guidance on CMC regulatory matters for investigational, new, and marketing products.Key ResponsibilitiesCMC Regulatory Strategy: Develop...

Job OverviewPosition: Regulatory Affairs Labeling SpecialistCompany: NovartisType: Temporary Contractor OpportunityAt Novartis, we are dedicated to improving the lives of millions around the globe. Every position, regardless of its nature, contributes significantly to our mission of enhancing human health.We collaborate with Magnit Global to provide flexible...

Job SummaryClinical Resource Network (CRN) is seeking a highly skilled CMC Regulatory Affairs Manager to join our team. As a key member of our regulatory affairs department, you will be responsible for providing strategic guidance on CMC regulatory matters for investigational, new, and marketing products.Key ResponsibilitiesCMC Regulatory Strategy: Develop...

Job OverviewPosition: Lead Regulatory Affairs ConsultantContract Duration: 12+ monthsCompensation: Up to $115/hrKey Responsibilities:The Lead Regulatory Affairs Consultant will leverage expertise in scientific, regulatory, and commercial aspects to ensure that i-STAT branded products comply with the necessary regulations in both the US and EU.This role...

Job OverviewPosition Title: Lead Regulatory Affairs ConsultantWork Schedule: Standard business hours, Monday to FridayROLE SUMMARY:The Lead Regulatory Affairs Consultant is responsible for integrating knowledge of scientific, regulatory, and commercial factors to ensure that i-STAT branded products developed, manufactured, or distributed by Point of Care...

About the RoleWe are seeking a highly experienced and skilled Executive Director to lead our Regulatory Affairs team in Precision Medicine & Digital Health. As a key member of our organization, you will be responsible for developing and executing global regulatory strategies to support the development of biomarkers, diagnostic tests, devices, and digital...

Position Overview:We are seeking a Senior Clinical Research Specialist to join our team at a leading Global Pharmaceutical Company. This role is focused on supporting the Center for Outcomes Research, Real-world Evidence, and Epidemiology (CORE) within Global Medical Affairs.Contract Details:This is a long-term contract position with the potential for...

Position Overview: The Senior Clinical Research Scientist plays a pivotal role within the Global Medical Affairs team, specifically supporting the Center for Outcomes Research, Real-world Evidence, and Epidemiology (CORE). This position is essential for driving the scientific understanding of product value and effectiveness in the healthcare landscape. Key...

The Director of Regulatory Strategy plays a pivotal role in overseeing the assigned brand initiatives and making all strategic decisions, including outlining the regulatory pathways for development. This position entails engaging with regulatory agencies, collaborating effectively with Contract Research Organizations (CROs), and liaising with various...

Position Overview:We are seeking a Senior Clinical Research Specialist to join our dynamic team at a leading Global Pharmaceutical Company. This role is integral to our Center for Outcomes Research, Real-world Evidence, and Epidemiology (CORE) team within Global Medical Affairs.Contract Details:This is a long-term contract opportunity with the potential for...