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Senior International Trial Manager for a Cardiovascular Outcomes Trial - Denmark  

Company managed [?] Still accepting applications

Posted on : 15 April 2017

Project Description


Job Description 
  • Do you want to be part of a team leading large global clinical trials to develop the world’s best diabetes treatments?
  • And do you like to work as a project manager with many stakeholders? Then a job as Senior International Trial Manager might be just the right job for you. 
  • 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 finalization 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. 



The position
  • In the job as Senior International Trial Manager you will work on a large global Cardiovascular Outcomes trial in obesity. 
  • 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 driving 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 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. 



Qualifications
  • You hold an academic degree within life science or healthcare. 
  • You have deep knowledge of clinical trial planning, execution and/or 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 skills. 
  • You are able to maintain overview, digest complex data and evaluate the adequate level of quality.



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.