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Medical Writer, Regulatory Documentation Specialist
2 months ago
Unlock Your Potential as a Medical Writer
Lundbeck is a leading innovator in neuro-specialty and neuro-rare fields, and we're seeking a talented Medical Writer to join our team. As a Medical Writer, you will play a crucial role in shaping the narrative of our clinical and regulatory documents, ensuring that scientific information and clinical data are presented clearly and concisely.
About the Role
You will be responsible for authoring high-quality documentation, including briefing documents, clinical trial reports, and Investigator's Brochures. Your expertise in regulatory medical writing will be invaluable in supporting our organization's strategy. You will work closely with colleagues in clinical, regulatory affairs, pharmacovigilance, and biometrics to ensure alignment and consistency in our documentation.
What We're Looking For
- At least 5 years of experience as a Medical Writer in the pharmaceutical industry
- PhD or master's degree in medical sciences, life sciences, or related areas
- Experience in advising and guiding clinical and regulatory teams on document content and processes
- Excellent analytical and communication skills
- Fluency in spoken and written English and a passion for writing
- Strong interpersonal and communication skills in a global environment
Why Join Us?
Lundbeck offers a dynamic and collaborative work environment, where you will have the opportunity to work on exciting projects and develop your skills. We are committed to building a diverse and inclusive workforce, and we welcome applications from talented individuals who share our values.
How to Apply
If you are a motivated and experienced Medical Writer looking for a new challenge, please upload your CV and a brief statement outlining your motivation for applying. We look forward to hearing from you
