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Are you adept at planning, coordination, problem-solving, and collaboration across the organization? Do you boast experience within clinical trial activities? Are you ready to take charge of operational clinical trial application (CTA) activities across the Novo Nordisk portfolio of projects and products? Then you might be the individual we are seeking in CTA Management. Apply now and carve your place in an exciting environment where driven individuals are dedicated to securing approval of Novo Nordisk’s Clinical Trials across the globe. The position
As an Associate Regulatory Professional for CTA Management at Novo Nordisk, you will have the opportunity to:

Foster cross-organizational collaboration and provide operational support to stakeholders in headquarters and affiliates.

Utilize your expertise in CTA local requirements to ensure compliance and successful submission to local authorities.

Participate in continuous improvement activities and projects within the department and across the organization, contributing to the development, optimization, and standardization of the CTA process.

Qualifications
From a successful candidate, we expect the following competencies:

A M.Sc. within natural sciences or a similar background (e.g., pharmaconomist, laboratory technician), or B.Sc. within natural sciences or a similar background with relevant experience working within Regulatory Affairs or Clinical Development/Clinic...