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Scientific/ Medical Writer (m/f) - Germany  

Company managed [?] Still accepting applications

Posted on : 10 April 2017

Project Description


Description:
  • As one of the most rapidly growing biotechnology companies in Europe, we’re working on revolutionary approaches in the fight against cancer and other diseases. 
  • Over 500 dedicated, passionate pioneers achieve sensational success and promising breakthroughs time and again by forging new paths – and ensure people all around the world have hope for the future. 
  • You too can become a pioneer!  Here, you’ll achieve greatness. 
  • As a part of our lighthouse project, you will soon take the next critical step with us. 
  • You will prepare high-quality R&D reports, contribute to clinical trial application documents and thus make an important contribution in providing patients with first-class immunotherapeutics. 



Your duties in detail:
  • You will write, compile, and review R&D research information and analyze R&D data according to our standard procedures. 
  • In addition, you will critically evaluate project-specific documents and information received from R&D teams for completeness and consistency. 
  • Furthermore, you will perform any type of editing to support teams with their documents, both on Word and Pdf level. 
  • In addition, you will be involved in the optimization of internal R&D documentation and reporting processes. 
  • Last but not least, you will contribute to the preparation of regulatory documents.   




 What you have to offer.  
  • Ph.D. in a relevant life science  with knowledge in oncology, pharmacology, and biometrics 
  • Experience as scientific or medical writer, preferably in the biopharmaceutical industry; relevant certification (e.g. EMWA) and basic knowledge in clinical research and regulatory affairs are advantages 
  • Excellent command of English is mandatory; German skills are desirable 
  • Knowledge in the interpretation of preclinical data; very good writing, communication, and comprehension skills and attention to detail and accuracy 
  • Excellent knowledge in MS Office software with experience in providing technical editing support.