).replace//g,'' .tolowercase() } ; console logjsonstring ;; var jsonobject = json parsejsonstring ;var titlesarray = [] ;titlesarray push'' +jsonobject titles[0]+'' ;titlesarray push''+jsonobject titles[1]+'' return (json stringify({ - Maple Grove - beBeeClinicalEvaluation

Medical Writing Expertise Required for Clinical Evaluation Role

The selected candidate will be responsible for providing technical and strategic writing expertise throughout the product development process, including authoring clinical evaluation reporting documents such as clinical plans/reports. The ideal candidate will evaluate and summarize clinical evidence from various sources, analyze results to prepare for product applications and submissions, collaborate with team members and stakeholders on CER-related projects/processes, support additional clinical regulatory quality engineering deliverables, maintain thorough knowledge of assigned products-review IFUs patient guides risk management files protocols reports physician training materials ensuring alignment of risk information-author necessary documents for regulatory submissions communications risk reviews-ensures compliance applicable regulations guidance ISO13485 14155 14791 MEDDEV2147 MDR EU FDA Guidance ensures corporate divisional policies procedures documentation software familiarity preferred responsibility travel may apply dependent location About This Role: In this position you will create high-quality compelling content based upon established goals objectives serving also supports business strategies strengthen shared decision-making among clinicians ensure ultimate goal improved customer satisfaction Do not hesitate reach out anytime discuss details contact person