Job Description
Requirement overview:
- Role: Scientific Writer – Clinical Narratives
- Number of resources: 2
- Duration: 12 months
- Location: Hyderabad Onsite
Scope of work:
The resources will be responsible for end-to-end development of patient safety narratives supporting Clinical Study Reports (CSRs) for submissions to regulatory authorities (e.g., FDA, EMA).
This includes:
- Drafting, editing, review, and finalization of narratives
- Interpreting data from clinical and safety databases
- Ensuring medical accuracy, clarity, and regulatory compliance
- Managing timelines and deliverables for assigned studies
- Performing quality control checks and ensuring formatting consistency
- Contributing to process improvement initiatives
- Given the natu...