Clinical Trial Coordinator

7 days ago


Ballerup, Ballerup Kommune, Denmark Novo Nordisk AS Full time

**Job Summary**

We are seeking a highly organized and detail-oriented Clinical Trial Administrator to join our Early Clinical Operations team at Novo Nordisk A/S. As a key member of our team, you will be responsible for supporting clinical trials in all aspects of study start-up, conduct, documentation, and archiving.

**Key Responsibilities**

  • Establish and maintain Trial Master Files in accordance with standard operational procedures (SOP) on different trials.
  • Update and upload information, index, and quality control trial documents in our IT Clinical systems.
  • Assist in outsourcing processes, trial budgets, and updating clinical documents such as protocol and protocol amendments.
  • Prepare monitoring guidelines, laboratory manuals, and enrolment updates in close collaboration with trial managers.
  • Support meeting planning and collaborate with internal and external stakeholders worldwide.

**Requirements**

  • Broad administrative experience from supportive roles, preferably within the pharmaceutical industry.
  • Flair for using IT systems and knowledge with Trial Master File systems, as well as high skills in MS Office, including Excel and Teams.
  • Strong team player with ability to work independently, well-structured with a sense for detail and good overview.
  • Good collaboration skills and a good sense of humor.
  • Proficient in both written and spoken English.

**About the Role**

This is a one-year maternity cover position based in Måløv, Denmark. As a Clinical Trial Administrator, you will be an essential member of our team, working closely with trial managers and stakeholders to ensure the smooth execution of clinical trials.



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