Submission Manager
Novo Nordisk
Are you passionate about clinical trial submissions? Do you possess a talent for oversee-ing project management and ensuring compliance with global requirements? If so, we have an exciting opportunity for you to join our team as a Submission Manager at Novo Nordisk. This is a great opportunity to be part of defining our future processes and make a difference for clinical trials teams. Read more and apply today for a life-changing ca-reer.The positionAs a Submission Manager at Novo Nordisk, you will lead and be accountable for the submission of initial Clinical Trial Applications (CTAs) and amendments to Health Authorities (HAs) and Ethics Committees (ECs) in alignment with business needs and priorities. This new role has been introduced to strengthen the current process and establish a center of excellence. We are looking for 4 people to join our team, and these positions will be based in Søborg, Denmark. You will collaborate closely with various stakeholders across Development and Affiliate to ensure timely and compliant submissions on a global scale.Your key responsibilities will include:
Qualification
To succeed in this role, you should:
As a person, you bring strong project management skills to the table, along with flexibility and cross-cultural awareness. You have the ability to inspire and motivate stakeholders, and your overall overview and analytical capabilities are exemplary. Moreover, your good communication, presentation, negotiation, and influential skills make you a valuable asset. Additionally, you possess the ability and willingness to adjust quickly to new situations in a continuously developing environment.
About the departmentYou will be part of a dynamic and dedicated team responsible for running all clinical devel-opment activities from initial planning of clinical trials towards authority submission. CTA Manage-ment is a department in constant development, and we are working closely with our stakeholders to continuously improve our processes to adapt and ensure compliance with the increasingly complex regulatory environment. Søborg, Hovedstaden
Wed, 11 Dec 2024 23:13:43 GMT
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