{"@context":"https://schema.org","@type":"JobPosting","title":"CER (Medical Writing) Professional","description":"

Writing and reviewing clinical/regulatory documents such as clinical trial protocols, Clinical evaluation reports, investigator brochures, informed consent forms, and according to ICH or other guidelines
CER - Medical Devices or IVD/IVDR (Clinical Evaluation) Module & Documentation writing
Publication manuscripts, abstracts, posters (content writing) and presentations participate in post-market surveillance activities by conducting routine systematic literature reviews (eg
Screening of articles against inclusion/exclusion criteria, extracting data from included studies, Interpreting study results and preparing summaries into formal reports) for specific medical device groups or subgroups
Develop templates for reports and other regulatory documents
Education & Qualifications:Any Bachelor / Master in Life Sciences Only
Required: a Minimum of 2 - 4 years of experience in Medical Writing (CER - Medical Devices or IVD/IVDR) or a related field

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