Medical Affairs Project Lead

Meet is seeking a seasoned Regulatory Affairs Director to lead their Regulatory Strategy projects across various therapeutic areas and modalities. This role will oversee all Regulatory Strategy initiatives, ensuring compliance and strategic alignment with the organization's goals.Key Responsibilities:Support clients with Regulatory Affairs projects,...

Director of Regulatory AffairsMeet is seeking a highly experienced Director of Regulatory Affairs to join their team. This role will oversee all Regulatory Strategy projects for the organization across a wide variety of therapeutic areas and modalities.Key ResponsibilitiesSupport clients with a variety of Regulatory Affairs projects (IND/CTA, NDA/BLA/MAA,...

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Job SummaryThe Medical Science Liaison (MSL) team at The Medical Affairs Company is seeking a highly skilled professional to join our team as a Medical Science Liaison for Endocrinology and Gastroenterology. This is a front-line field position, critical to establishing and maintaining excellent educational and research collaborations with healthcare...

Director, Regulatory Affairs - Small Molecule StrategyMonte Rosa Therapeutics is a clinical-stage biotechnology company developing innovative therapies for patients living with serious diseases in oncology, autoimmune, and inflammatory diseases, and more.The successful candidate will be responsible for developing and implementing regulatory strategies to...

Job Title: Medical Science Liaison for Endocrinology and GastroenterologyThe Medical Science Liaison (MSL) team at The Medical Affairs Company is responsible for establishing and maintaining relationships with healthcare professionals (HCPs) to educate and provide information on our company products. The MSL will develop and build relationships with national...

About the RoleWe are seeking a highly skilled Associate Director, Global Regulatory Affairs Marketed Products to join our team at Takeda Pharmaceutical. As a key member of our regulatory affairs team, you will be responsible for defining, developing, and leading global strategies to maximize regulatory success for our marketed products.Key...

Medical Asset Strategy DirectorProclinical Staffing is seeking a Medical Asset Strategy Director to oversee a dedicated team and drive the medical plan for oncology assets.Key Responsibilities:This role will involve leading the creation and communication of the integrated asset medical data generation plan, ensuring alignment with functions prior to Asset...

Job Title: Senior Manager, Regulatory AffairsJob Summary: We are seeking a highly skilled and self-motivated regulatory professional to join our team. This role will focus on oncology, immunology, and related therapeutic areas.The successful candidate will be responsible for developing and implementing regulatory strategies to support the global development...

About the RoleWe are seeking an experienced Associate Director, Scientific Communications Lead, Solid Tumors to join our team. As a key member of our Global Medical Affairs Oncology team, you will be responsible for developing and executing strategic publication plans and scientific communication strategies for our assigned oncology assets.Key...

Job Summary Precision for Medicine, Manufacturing Solutions is seeking a Senior Project Engineer to join our team. As a leader in the life science industry, we are committed to advancing manufacturing to achieve operational excellence and accelerate speed to market for next-generation medicines.Key Responsibilities Create alignment with cross-functional...

About the Role:At Takeda, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients worldwide.As a Manager,...

Job Title: Director, Regulatory StrategyAt Inozyme Pharma, we are seeking a highly experienced and skilled Director of Regulatory Strategy to join our team. As a key member of our regulatory affairs team, you will play a critical role in driving the development and execution of regulatory strategies for our rare disease therapeutic programs.Key...

Job Summary:The College of Charleston seeks a highly qualified Vice President of Academic Affairs to lead its academic programs and initiatives. This senior leadership role is responsible for overseeing the academic integrity and excellence of the institution, providing strategic direction for academic programs, policies, and initiatives, and ensuring...

About the RoleAt Takeda Pharmaceutical, we are a forward-looking, world-class R&D organization that unlocks innovation and delivers transformative therapies to patients. By focusing R&D efforts on four therapeutic areas and other targeted investments, we push the boundaries of what is possible in order to bring life-changing therapies to patients...

Job Title: Lead Mission DesignerJob Description:The Molasses Flood, a CD PROJEKT game development studio, is seeking a Lead Mission Designer to join their team. As a key member of the design team, you will be responsible for creating engaging and replayable multiplayer experiences for a brand new adventure set in The Witcher universe.Responsibilities:Manage...

Lead Mission DesignerWe are seeking a highly skilled and experienced Lead Mission Designer to join our team at CD Projekt. As a key member of our design team, you will be responsible for creating engaging and replayable multiplayer experiences for our upcoming game set in the Witcher universe.Key Responsibilities:Manage a team of mission designers to create...

Senior/Principal Gameplay EngineerThe Molasses Flood, a renowned CD PROJEKT game development studio based in the greater Boston area, seeks an experienced Senior to Principal Gameplay Engineer to contribute to the development of our latest project, a new multiplayer title set within the world of The Witcher.This role is a great opportunity for skilled...

Job SummaryAs a Director, Regulatory Affairs CMC Small Molecules at Takeda, you will oversee the development and execution of regulatory CMC development and registration strategies. You will be responsible for leading cross-functional teams and communicating with international Health Authorities as necessary. This role requires a high level of leadership and...

Unlock Your Potential as a Senior Project Manager at Genioo AGAs a Senior Project Manager at Genioo AG, you will have the opportunity to work with high-profile clients in the life sciences industry. You will be part of a consulting team that specializes in supporting companies in designing and executing complex projects. Your role will involve managing...