📑 Job PurposeThe Clinical Science Specialist will provide appropriate leadership and management within Clinical Development, to provide scientific and clinical development support for products within MoonLake Immunotherapeutics assigned therapy area.Key responsibilities:Support development and execution of med ...
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📑 Job PurposeAs a Global Clinical Project Manager you are responsible for the management of all aspects of the Clinical Study Team activities for assigned clinical studies. The Global CPM, in concert with the Director Clinical Operations, is accountable for achieving successful execution and delivery of Moonlake´s clinical development team activities ...
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📑 Job PurposeAs the Clinical SAS programmer you will contribute to the oversight of vendor programming activities and perform exploratory analyses of completed and ongoing MoonLake sponsored clinical trials to provide insight and to ensure high quality data, datasets and statistical outputs.Key accountabilities:<b ...
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📑 Job PurposeAs a Global Clinical Project Manager you are responsible for the management of all aspects of the Clinical Study Team activities for assigned clinical studies. The Global CPM, in concert with the Director Clinical Operations, is accountable for achieving successful execution and delivery of Moonlake´s clinical develop ...
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📑 Job PurposeThe Medical Director will serve as medical lead for MoonLake’s clinical development programs and as medical advisor to the Executive team and all internal functions regarding clinical development activities. Key Responsibilities:Provides medical oversight of outsourced study conduct including interactions with CRO medical and drug safet ...
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📑 Job PurposeThe Clinical Supply Chain Manager is responsible for coordination of all supply matters for clinical and future commercial supply, including distribution of a MoonLake product that helps improve the lives of patients worldwide.Key AccountabilitiesThe supply chain manager is key leader for:Driving detailed planning, scheduling and order m ...
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📑 Job PurposeThe Medical Director will serve as medical lead for MoonLake’s clinical development programs and as medical advisor to the Executive team and all internal functions regarding clinical development activities. Key Responsibilities:Provides medical oversight of outsourced study conduct including interactions ...
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📑 Job PurposeAs a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development team responsible for the development, execution and tracking of regulatory CMC and medical device activities.You will be responsible for the development of a CMC and device regulatory strategy, working closely with Technical Operation ...
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📑 Job PurposeThe Clinical Supply Chain Manager is responsible for coordination of all supply matters for clinical and future commercial supply, including distribution of a MoonLake product that helps improve the lives of patients worldwide.Key AccountabilitiesThe supply chain manager is key le ...
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📑 Job PurposeAs a Senior Manager, Regulatory Affairs CMC, you are an integral part of MoonLake’s Clinical Development team responsible for the development, execution and tracking of regulatory CMC and medical device activities.You will be responsible for the development of a CMC and device regulatory strategy, working closely with Tec ...
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📑 Job PurposeThe Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development team. You will lead the development of content for submissions to regulatory agencies and other external stakeholders.This role will partner closely with key internal and external stakeho ...
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📑 Job PurposeAs a Senior Quality Expert (GCP), you will support senior management in ensuring Quality is at the heart of all company initiatives and, specifically, you will act as advisor to the Clinical Development teams on all quality related GCP activities.Key accountabilities: ...
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📑 Job PurposeThe Senior Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development team. You will lead a team responsible for developing the content for submissions to regulatory agencies and other external stakeholders.This role will partner closely with key internal and external stakeholders and requires crit ...
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📑 Job PurposeAs a Senior Quality Expert (GCP), you will support senior management in ensuring Quality is at the heart of all company initiatives and, specifically, you will act as advisor to the Clinical Development teams on all quality related GCP activities.Key accountabilities:To play a key role in maintaining and monitoring the GxP Quality Manage ...
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📑 Job PurposeThe global safety scientist role is responsible for providing scientific expertise to safety surveillance and risk management activities for MoonLake products in clinical development. The role actively contributes to setting the strategic direction within drug safety and to the development of safety standards and proc ...
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📑 Job PurposeThe Senior Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development team. You will lead a team responsible for developing the content for submissions to regulatory agencies and other external stakeholders.This role will partner closely with key internal and externa ...
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📑 Job PurposeThe Manager, Medical & Regulatory Writing will be an integral part of MoonLake’s Clinical Development team. You will lead the development of content for submissions to regulatory agencies and other external stakeholders.This role will partner closely with key internal and external stakeholders and requires critical thinking along with e ...
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📑 Job summary This post is a full time appointment for an initial period of 12 months with potential to extend to 24 months. The role to provide medical support to the Early Phase Trials team including consultants, nursing and administration staff by primarily acting as co-investigator on early phase clinical trials. Th ...
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