Senior Global Trial Manager - Cardiovascular

at  Novo Nordisk

Senior Global Trial Manager - Cardiovascular
Category: Clinical Development
Location:Søborg, Capital Region of Denmark, DK
Do you want to make a difference to both people and society?
Do you dream of becoming part of international clinical trial teams as we set out on a journey into new and exciting therapeutic areas within cardiovascular diseases?
Can you help us bring new treatments to patients, faster and smarter, having a strong focus on the patient perspective by leading and optimizing trial work within your area of expertise?
Then you could be our new Senior Trial Manager in an exciting project in cardiovascular, kidney and Alzheimer’s disease area.
Working at Novo Nordisk is never just a job. Apply now for a life-changing career.

QUALIFICATIONS

We realise that few people are experts at everything. But if you have the following qualifications, then you could be the person we are looking for:

• Master’s degree in Natural Science with several years of relevant experience, or a bachelor’s degree with at least three years of relevant
• Experience from working in or collaborating with Clinical Research Organisations
• Knowledge and experience in clinical trial methodology combined with creativity, flexibility, and an infectious can-do attitude
• Confidence and personality to drive changes in the way we work across skill types
• A track record in planning, execution, and follow-up of clinical trials is required, with a creative and innovative attitude that will enable you to drive initiatives with operational excellence in mind

As a person, you are a high performer with excellent communication, presentation and negotiation skills. You create consensus across professional and geographical borders and build trust among colleagues to establish mutually profitable working relationships.

• Ensuring trial progress with a strong patient focus throughout the project and driving change based on patient insights
• Vendor Management including collaboration with Clinical Research Organisations and monitoring deliverables
• Preparing materials for internal reviews and trial partner meetings
• Actioning and tracking deviations and amendments
• Support initial trial-specific setup of Clinical Trial Management System (CTMS), coordinating country/site level CTMS setup, establishing and maintaining Trial Master Fil