Medical Affairs Director for Rare Diseases

{"Job Title": "Associate Director, Medical Affairs, Adult Cholestatic Diseases", "Job Summary": "We are seeking a highly skilled Associate Director to join our Medical Affairs team in Cambridge, MA. As a key member of our team, you will be responsible for contributing to the medical strategies and overall US medical affairs plan for adult cholestatic...

Job Title: Associate Director Medical Affairs Adult Cholestatic DiseasesCompany: Ipsen Biopharmaceuticals IncLocation: Cambridge, MA, United StatesJob Description:Job Summary:The Associate Director Medical Affairs Adult Cholestatic Diseases will support and oversee some of the medical affairs activities of the adult cholestatic therapeutic areas. This role...

About the RoleWe are seeking a highly skilled Associate Director, Medical Affairs, Adult Cholestatic Diseases to join our team at AAPC. As a key member of our Medical Affairs department, you will play a critical role in supporting and overseeing medical affairs activities for adult cholestatic therapeutic areas.Key ResponsibilitiesContribute to and lead...

About the RoleWe are seeking a highly skilled and experienced Director of Dermatology Medical Affairs to join our team at Takeda. As a key member of our US Medical Affairs organization, you will be responsible for developing and executing medical strategies for our dermatology products.Key ResponsibilitiesDevelop and execute medical strategies for assigned...

Job Title: Senior Associate Scientist, Rare Disease ResearchWe are seeking a highly motivated and experienced Senior Associate Scientist to join our Rare Disease & Neurology (RD&N) Research Unit at Biogen. As a key member of our team, you will contribute to advancing research for drug discovery and development programs in rare neurological disorders.Key...

Job TitleSenior Director of Clinical AffairsJob SummaryWe are seeking a highly experienced and skilled Senior Director of Clinical Affairs to join our team at Philips. As a key member of our organization, you will be responsible for delivering clinical knowledge, experience, and expertise across the entire value chain from ideation to end-of-life.Key...

Job Title: Medical Director, Alzheimer's, US Medical AffairsBiogen is seeking a highly skilled Medical Director to lead the development and execution of the US medical strategy for Alzheimer's. As a key member of the US Specialty Care Medical Director office team, you will be responsible for supporting the development and implementation of the US Medical...

The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and leads regulatory projects across various development phases. This position demands a strategic regulatory expert who will guide drug development initiatives, leveraging extensive expertise to inform project teams on compliance requirements and...

The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and as a leader in regulatory projects across various development phases. This position is essential for guiding drug development initiatives and leveraging extensive regulatory knowledge to support project teams in navigating complex...

The Director of Regulatory Affairs at The Steely Group plays a pivotal role as a liaison with Health Authorities and leads regulatory projects across various development phases. This position demands a strategic regulatory leader who can effectively guide drug development initiatives by leveraging extensive expertise in regulatory frameworks.Key...

Job Description**About the Role**We are seeking an experienced Executive Director of Market Access and Public Policy to lead the strategic development and execution of market access and public policy initiatives to ensure the successful launch and sustainable patient access of our innovative gene editing medicines in both ex vivo and in vivo applications.Key...

Job SummaryWe are seeking an experienced Associate Director, Global Medical Information to join our team at AAPC. This individual will be responsible for providing timely, evidence-based, and fair-balanced medical information to external customers and internal stakeholders.Key ResponsibilitiesAdvance Medical Information Business Processes: Develop and...

About the RoleWe are seeking a highly skilled and experienced Regulatory Affairs Director to join our team at GlaxoSmithKline. As a key member of our Global Regulatory Affairs team, you will play a critical role in shaping our regulatory strategy and ensuring compliance with regulatory requirements.Key ResponsibilitiesDevelop and implement regulatory...

About This RoleThe Associate Director, Marketing - Social Media will be a critical role and visible leader within the North American Organization leading the overall HCP and patient/caregiver social media strategies. This individual will be responsible for driving innovative social media engagement initiatives for HCPs, patients, and families maximizing...

Regulatory Affairs Director, Small MoleculesTakeda is seeking a highly experienced Regulatory Affairs Director, Small Molecules to lead our Global Regulatory Affairs CMC team. As a key member of our team, you will be responsible for overseeing the development and execution of regulatory CMC development and registration strategies.Key Responsibilities:Plan,...

About the RoleWe are seeking a highly skilled Associate Director, Global Medical Communications to join our team. As a key member of our Global Medical Affairs department, you will play a critical role in developing and executing medical communication strategies across various disease areas.Key ResponsibilitiesDevelop and implement global medical...

About the RoleThe Associate Director, Global Medical Communications is a strategic role within Global Medical Affairs that collaborates with cross-functional partners to oversee one or more disease areas/assets on a Global level.Key ResponsibilitiesDevelop and execute medical communication plans encompassing tactics such as core content, scientific...

Job SummaryWe are seeking a highly experienced and skilled Director of Regulatory Affairs and Quality to lead our Regulatory Affairs and Quality teams in the development and execution of compliant regulatory strategies and quality team/QMS responsibilities.Key ResponsibilitiesRegulatory Affairs Strategy and ExecutionDevelop and execute end-to-end regulatory...

Job Title: Senior Director, Regulatory AffairsApnimed is a clinical-stage pharmaceutical company dedicated to transforming the treatment of sleep apnea. We are seeking a highly experienced Senior Director of Regulatory Affairs to play a key role in advancing our innovative programs through clinical trials and commercialization globally.Key...

About the RoleWe are seeking a talented and motivated Principal Software Product Manager to join our team at the Broad Institute. As a key member of our leadership team, you will be responsible for synthesizing the needs and goals of various stakeholders into a highly engaging product platform.Key ResponsibilitiesStrategize with CMI leadership to set the...