required for CE marked devices Responsible for writing Clinical Investigation Plans Provide clinical input and standards (ISO 14155) Experience in medical writing, conducting systematic review and clinical data confidential information Excellent scientific writing / report writing skills Communication skills (written and
required for CE marked devices Responsible for writing Clinical Investigation Plans Provide clinical input and standards (ISO 14155) Experience in medical writing, conducting systematic review and clinical data confidential information Excellent scientific writing / report writing skills Communication skills (written and