Seeking a Director - Global Regulatory Lead to lead a global regulatory team in developing and executing regulatory strategies for high impact projects. Responsibilities include leading health authority interactions, managing global filing activities, presenting regulatory strategies, and conducting regulatory reviews.

Lead the evaluation of digital/data assets for Novo Nordisk, collaborate with internal stakeholders, and shape the approach for acquiring external innovation. Develop and implement a strategy for evaluating and acquiring digital assets aligned with the company's objectives and growth initiatives.

The project manager will implement IT projects within business applications and IT infrastructure to support the business in the Novo Nordisk Lexington, Massachusetts site in close collaboration with global partners, business partners, and IT. This position will work across Novo Nordisk departments and locations, managing projects benefitting various functions such as Research, Early Development, Clinical Operations, Quality, Manufacturing, Supply Chain, Finance, Facilities, IT, and others. Responsibilities include initiating new business and IT projects, planning and coordinating project deliverables, leading project scope and deliverables definition, and managing risks.