Medical Writing Expert for Clinical Disclosure

17 hours ago


Copenhagen, Copenhagen, Denmark LEO Pharma Full time

Your Role: As a Medical Writing and Clinical Disclosure Professional, you will play a crucial part in planning, managing, and writing clear, concise, and audience-friendly regulatory, scientific, and medical documents. Your main tasks will include:

  1. Writing and editing original regulatory, scientific, and medical documents at a professional level.
  2. Leading and managing the preparation of documents in cross-functional teams.
  3. Overseeing clinical trials conducted by vendors.
  4. Facilitating redaction and anonymization of clinical documents.
  5. Maintaining accuracy of our externally facing website: leopharmatrials.com.
  6. Contribution to regulatory submissions to health authorities.

Your Qualifications: To succeed in this role, we imagine that you have the following qualifications:

  1. A university degree in health or biological science (MSc, MD, or equivalent).
  2. Research experience and experience with writing publications for scientific journals.
  3. The ability to plan, handle, manage, structure, and write clear, concise, and audience-friendly regulatory, scientific, and medical documents fit for purpose.
  4. Knowledge of clinical development, GCP, scientific research methods, and applicable regulatory guidelines.
  5. Experience with or interest in regulatory requirements within clinical disclosure and associated disclosure tasks.
  6. Fluent in oral and written English and a passion for writing.


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