Clinical Publisher

at  Novo Nordisk

Søborg, Region Hovedstaden, Denmark -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate06 Feb, 2025Not Specified06 Nov, 2024N/ADocumentation,Editing,Excel,Instructions,Harmony,Customer Service,EnglishNoNo
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Description:

Clinical Publisher
Category: Clinical Development
Location:Søborg, Capital Region of Denmark, DK
Are you a fast learner and interested in clinical development and documentation? Do you have a quality mindset and a flair for learning new software? We are now looking for a Clinical Publisher for our clinical publishing team in Søborg.
Apply now for a life-changing career!

QUALIFICATIONS

As an individual, you are structured, detail oriented, proactive and service-minded. You like following instructions, and you take great pride in what you do. You can maintain an overview while managing diverse tasks and effectively prioritize. Possessing a quality mindset is essential, and you have a track record of meeting deadlines. You work independently, yet you also thrive as a natural team player, consistently contributing to the success of any team you are involved with.

We’re seeking candidates who fulfil the following prerequisites:

  • MSc or a similar degree
  • Extensive experience in use of Document Management Systems.
  • Experience in editing and preparing documentation in Excel, Word, and Adobe Acrobat Pro and proficient in PowerPoint, SharePoint and O365 apps.
  • Be a fast learner with an eye for detail and the ability to quickly pick up new software skills.
  • Be flexible and structured and be able to thrive in a fast-changing work environment while maintaining ambitious standards of accuracy, quality, and customer service to stakeholders.
  • Be proactive, capable of working independently, and able to prioritise and plan your own tasks, while at the same time being an active contributor to the success and harmony of the entire team.
  • Be a skilled communicator who is fluent in both written and spoken English.
  • Experience from working in the pharmaceutical or publishing industries will be preferred.

Responsibilities:

  • Electronic quality control of documents to ensure adherence to regulatory requirements such as file size, bookmarks, links, margins, etc.
  • Supporting our clinical organisation in the use of various databases and templates to store clinical information.
  • Engaging in projects developing and implementing digital solutions for publishing.
  • Supporting medical writers, affiliates, trial managers, and other colleges in our clinical processes


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Pharma / Biotech / Healthcare / Medical / R&D

Clinical Pharmacy

MSc

Proficient

1

Søborg, Denmark