Medical Writer

For one of our clients located in Darmstadt (Germany), we are actively looking for a Medical Writer.

  •  Do you have experience in Medical Writing, Regulatory Submissions, Writing strategic documents ?
  •  Do you have a strong English knowledge - written and spoken ?
  •  Are you willing to work 80% on site and 20% remotely ?

Then, don't wait anymore and apply today!

Job Description 

The Medical Writer brings his writing skills in the R&D/Clinical Development area. He/She will report to the Director, Medical Writing, non-Oncology. The non-Oncology group focuses on projects in the following therapeutic areas; Immunology, Neurology, Fertility, Healthy Volunteer Trials, Regional/Local Studies. 

Responsibilities 
  •  You oversee and coordinate the preparation of documentation for regulatory submissions (e.g., investigator brochures, protocols, and clinical study reports) in collaboration with other team members or CROs
  •  You write strategic submission documents (e.g., IMPDs, briefing documents, clinical summaries) with the aim to ensure the quality of documents
Profile 
  • You have experience in Medical Writing, Regulatory Submissions, Writing strategic documents 
  • You have a strong English knowledge - written and spoken 
  • You are willing to work 80% on site and 20% remotely
  • You have good communication skills and you are a real team player
  • You are stress-resistant
  • You have an eye for detail, you are quality-oriented
  • You have very strong organization and time management skills 
Contact Information 

Amandine Planche
+32 10 68 53 30
amandine.planche@valesta.com

Application form : Medical Writer

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