Clinical Development Documentation Specialist
Acts as a key internal support for the Clinical Development Group with respect to preparing and managing technical documents, SharePoint [intranet] sites, and imaging databases. Responsible for the administration of technical documentation and their revision control for a family of products over their lifecycles. This role will include data entry and spreadsheet management for pre-clinical and clinical study results, post-market surveys, and design validations. Will also support IFU (Instruction for Use) change history documentation, scientific literature compilation and case study imaging Read more […]