Qualifications:

• Experience in medical writing or demonstration in scientific writing ability is 
   required.
• Able to quickly develop therapeutic expertise across medical device 
   portfolios, business objectives, clinical data/evidence is required.
• Strong oral communication, presentation, project management and 
   prioritization skills are required.
• Excellent interpersonal relationship skills are required.
   Experience within the medical device industry and knowledge of CER 
   regulatory requirements, evidence generation, and CER document creation is 
   preferred.
• Ability to understand and interpret statistical results of clinical studies and 
  understand good data management practices is preferred.
• High proficiency in Microsoft Office Suite is preferred.

Requirements:

Minimum of 3 to 5 years of relevant experience in identified functional 
domain/business workstream for non-MD; 1 year experience for MD

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