Medical Writer |Jr Level| Hyderabad
Writing and reviewing clinical/regulatory documents such as clinical trial protocols, clinical studyreports, investigator brochures, informed consent forms, and according to ICH or other guidelines.
Minimum of 0.6 - 3 years of experience.
Module Drafting (2.4, 2.5. 2.6 2.7).
Publication manuscripts, abstracts, posters (content writing) and presentations
To participate in post-market surveillance activities by conducting routine systematic literature reviews(e.g. Screening of articles against inclusion/exclusion
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Minimum of 0.6 - 3 years of experience.
Module Drafting (2.4, 2.5. 2.6 2.7).
Publication manuscripts, abstracts, posters (content writing) and presentations
To participate in post-market surveillance activities by conducting routine systematic literature reviews(e.g. Screening of articles against inclusion/exclusion