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CER (Medical Writing) Professional
DDi LLC · Hyderabad · onsite · Posted 66d ago
Undisclosed3–6 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
- 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
Sourced from naukri
Skills
medical writingCERCER writingmedical careMedical DevicesContent WritingLife Sciences