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