Senior Global Trial Manager – Cardiovascular

Job title:

Senior Global Trial Manager – Cardiovascular

Company:

Novo Nordisk

Job description

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Accept ClosePress Tab to Move to Skip to Content LinkSearch by KeywordSearch by LocationLoading…CategorySelect how often (in days) to receive an alert:×Select how often (in days) to receive an alert:Senior Global Trial Manager – CardiovascularCategory: Clinical DevelopmentLocation:Søborg, Capital Region of Denmark, DKDo 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 the Ziltivikemab 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.The position
As a Senior Global Trial Manager, you will be responsible for securing the successful delivery of significant trial management elements. You will have the responsibility for tasks from trial start-up, during conduct and through the closeout stages of the trial. You will have the chance to constantly pursue, develop and implement new and better clinical trial practices and share them with your team.Your main responsibilities will include:

• 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 File

You will also drive your tasks forward with the right stakeholders and take responsibility for close stakeholder collaboration and clear communication, e.g. during Monitor Meetings and Investigator Meetings, while escalating issues as necessary based on project work plansThe job is based in Søborg, Copenhagen area, Denmark and has a global scope. Therefore, travelling for meetings will be part of the job. We are happy to discuss flexible working, depending on the role and subject to business needs.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.About the department
Clinical trial operation activities are anchored in the Clinical Drug Development organisation and play a vital part in our ambitious drug development program. We plan and execute global clinical trials to produce the high-quality data and scientific documentation required by health authorities to turn our promising pipeline of exciting new medicines into marketable products. As a Senior Trial Manager, you may be working on trials ranging from small and complex projects to large cardiovascular outcome projects. Taking on this international role is a unique opportunity to make an impact and boost your career in a large and resourceful global development organisation.Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive it. We’re a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care.Contact
For further information or to get to know us better please .Deadline
07 October 2024Please note that applications will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible.We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.

Expected salary

Location

Søborg, Hovedstaden

Job date

Fri, 20 Sep 2024 04:41:42 GMT

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