- 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

📌 CER (Medical Writing) Professional (Hyderabad)
🏢 DDI India
📍 Hyderabad