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International Trial Managers for Cardiovascular Outcomes Trials Søborg Denmark,  

Novo Nordisk (company)

Posted on : 15 April 2017

Project Description

Job Description
  • Do you have a passion for planning and driving clinical trials, and do you want to be part of a team leading large global clinical trials to develop the world s best diabetes treatments? 
  • Then we may have just the right job for you. Trial Operations, Semaglutide Diabetes & Diabetes Outcomes is looking for an International Trial Manager. 
  • In Global Development, we are responsible for managing clinical drug development worldwide from early development phases to life-cycle management. 
  • We ensure medical and scientific documentation for clinical submissions and authorities while ensuring that the process lives up to uniform global standards, regulations and business ethics.

About the department
  • In Trial Operations, Semaglutide Diabetes & Diabetes Outcomes, we are approximately 75 highly skilled and ambitious employees. 
  • We are responsible for the planning, execution and finalisation of clinical trial activities and for conducting large cardiovascular outcomes trials in diabetes and obesity. 
  • Further, we collaborate with external vendors, and our colleagues in the company  affiliates worldwide. 
  • We value an open, trust-based and creative working environment, great team spirit and a high quality mind-set. 
  • We offer unique opportunities for you to play an important role in our evermore imperative work of bringing new and better treatments to the market.

The position
  • In the job as International Trial Manager you will work on a large global Cardiovascular Outcomes trial. 
  • The job demands that you are capable of directing and driving activities within global clinical trials. 
  • You will be responsible for ensuring that project key deliverables are met in time, are of high quality and within budget. 
  • You will be part of the international study group, where you will contribute to planning and conducting team meetings with focus on stakeholder engagement, knowledge sharing and decision making.
  • The job requires that you apply a structured and analytical approach during development of relevant trial documents such as trial protocol, informed consent, recruitment strategies, risk analysis plans, communication plans and trial budgets. 
  • You are detail-oriented, while able to maintain overview, digest complex data and evaluate the adequate level of quality. 

  • You hold an academic degree within life science or healthcare.
  •  You have knowledge of clinical trial planning, execution and finalization.
  •  Further, you have experience in ensuring that your stakeholders deliver their best in an ever-changing environment.
  •  The job requires proficiency in English.
  •  You work independently while also being a dedicated team player and have good cross-cultural awareness skills.

Working with Us:
  • Your skills, dedication and ambition help us change lives for the better.
  • In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.
  • We invest significantly in both professional and personal development and the position offers attractive career opportunities for both internal and external candidate.


Denmark Søborg

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