Regulatory Affairs Manager - Danbury, CT

'Working at Yale means contributing to a better tomorrow. Whether you are a current resident of our New Haven-based community-eligible for opportunities through the New Haven Hiring Initiative or a newcomer interested in exploring all that Yale has to offer your talents and contr ...

This role is based in Purchase, NY and will require a good amount of travel in the Northeastern United States (NY, NH, CT MA RI ME VT) PepsiCo products are enjoyed by consumers more than one billion times a day in more than 200 countries and territories around the world. · The Pu ...

This role is based in Purchase, NY and will require a good amount of travel in the Northeastern United States. · ...

This role is based in Purchase, NY and will require a good amount of travel in the Northeastern United States (NY, NH, CT, MA, RI, ME, VT). The Public Policy and Government Affairs (PPGA) team helps PepsiCo navigate the increasingly volatile and complex policy and regulatory land ...

This position will mainly be responsible for leading development of scientific health and nutrition dossiers and outreach efforts to healthcare professionals for our U.S. Danone businesses. · Develop scientific health and nutrition dossiers to substantiate consumer messaging and ...

The Manager of Faculty Affairs will report directly to the Director of Faculty Affairs and will collaborate with the Finance & Administration teams, Faculty and Staff in the IBO (Integrated Business Operations), and Yale School of Medicine (YSM) Institutional offices. · ...

+Job summary · The Regulatory & Clinical Affairs Manager is responsible for overseeing regulatory compliance and clinical affairs activities across the product lifecycle.This role serves as a key liaison between internal leadership, clinical consultants, quality, and external reg ...

+The Regulatory & Clinical Affairs Manager is responsible for overseeing regulatory compliance and clinical affairs activities across the product lifecycle. · +Manage administrative aspects of clinical trial and clinical affairs activities. · Facilitate communication and coordina ...

The Regulatory & Clinical Affairs Manager oversees regulatory compliance and clinical affairs activities across the product lifecycle. · ...

The Regulatory & Clinical Affairs Manager is responsible for overseeing regulatory compliance and clinical affairs activities across the product lifecycle. · ...

Regeneron is seeking a Manager, of Advertising and Promotion to join our Regulatory Affairs team · In this role, a typical day might include: · The Manager position within the Regulatory Affairs department requires the ability to apply clinical development knowledge in concert wi ...

The Program Manager is responsible for providing direct supervision of the program.This position manages programs and projects by reviewing, analyzing and evaluating operations to ensure proper management and effective operations. · Lead strategic faculty-related projects across ...

Support the Senior Director in developing and executing regional regulatory strategies for QOL. · Contribute to providing strategic oversight and leadership to the regulatory team, · ensuring alignment with company objectives and regional regulatory requirements. ...

· Description · Responsible for independently leading and coordinating the global compilation and worldwide submission of dossiers for new chemical and biological marketing authorization applications, complex life cycle dossiers, original INDs, and the related health authority r ...

The Regulatory & Clinical Affairs Manager oversees regulatory compliance and clinical affairs activities across the product lifecycle. This role serves as a key liaison between internal leadership, clinical consultants, quality, and external regulatory authorities. · The position ...

The Senior Manager position within the Regulatory Affairs department requires the ability to apply clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidance to the development of key product messages presented in Bi ...

+The Senior Manager position within the Regulatory Affairs department requires clinical development knowledge in concert with experienced understanding of advertising and promotion regulations/guidance to develop key product messages presented in Biologic License Applications (BL ...

+The Senior Manager, Regulatory Affairs will report to the Global Regulatory Liaison (GRL) and provides support to the GRL in all aspects of regulatory affairs related to the development of novel therapeutics including quality, preclinical and clinical areas of drug development a ...

The Senior Manager, Regulatory Affairs will report to the Global Regulatory Liaison and provides support in all aspects of regulatory affairs related to drug development and compliance with regulations. · Coordinate the preparation and submission of global regulatory submissions ...

The Operations Manager supports both VPIA and the MacMillan Center at an estimated 80% -20% split. This role will provide high level financial management, business information and forecasting needs for the various programs housed within VPIA including the Office of International ...