Trial Project Manager to lead and take overall responsibility for global clinical trials

  • Clinical Development and Medical
  • Søborg

 

   

Do you dream of leading and optimizing international clinical trials as we set out on a journey into new and exciting therapeutic areas and ways of working? Can you bring new treatments to patients, faster and smarter? Then you could be our new Trial Project Manager.



About the department
Clinical trial operation activities are anchored in the R&D organisation under Global Development and play a vital part in our ambitious drug development program. We plan and execute 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 Trial Project Manager, you may be leading trials ranging from small and complex haemophilia projects to large cardiovascular outcome projects. Taking on this central, international role is a unique opportunity to make an impact on a large and resourceful global development organisation.

 

The position
As Trial Project Manager, you will be leading and overseeing up to 3 clinical trials concurrently. You’ll assume the overall accountability for the trials from the early start to overseeing close-down, making sure all data, documents and sensitive information is secured. Continuously driving trials forward, you ensure that all parties communicate, coordinate and collaborate according to plan. You should walk the talk when it comes to constantly learning and driving change in how we run clinical trials at Novo Nordisk. Everything from creating efficiency and speed to how we implement our digital strategy is on the table. Your success indicators also include:

  • Identifying issues and threats to timeliness and mitigating them
  • Driving and providing operational input to new clinical assessments
  • Ability to drive implementation of our digital strategy
  • Building excellent third-party relations

 

The job is based in Denmark but has a global scope. Travelling for meetings will be part of the job.

 

Qualifications
You hold a MSc in Natural Science with several years of relevant experience, or a BSc in Natural Science or equivalent with several years of relevant experience. You have in-depth knowledge about clinical trial methodology and solid experience in project managing clinical trials. Most importantly, you bring creativity, flexibility and an infectious can-do attitude to clinical trials. You have the confidence and personality to drive changes in the way we work across skill types.

 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 throughout the organization. When dealing with external parties, you come across with confidence and openness, always looking for solutions that benefit both parties and position Novo Nordisk as an attractive collaborator.

 

Working at Novo Nordisk
At Novo Nordisk, we are the world leader in diabetes care and a major player in obesity treatment, haemostasis management, growth hormone therapy and hormone replacement therapy. Our R&D and production facilities span five continents and our people are united by their passion for creating sustainable solutions.
 

Contact
For further information, please contact Julie Ziegler Beckman at +45 3079 6903 or Dorthe Lyngsø Vuylsteke +45 3075 5078.

 

Deadline
12 July 2020 but we will screen and interview on an ongoing basis.

 

 

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.


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