Medical Writer

1. Writing, editing, reviewing, formatting, publishing regulatory (clinical and post marketing) documents and dossier sections in a manner compliant with FDA, EMA, CDSCO, ICH, CONSORT guidelines and other similar standards.

2. Collaborating with the clinical team in developing and strategizing the Clinical Development Plan.

3. Collaborating across line functions in preparing SOPs for Regulatory documents.

4. Interpreting, representing and summarizing clinical and scientific data.

5. Planning, organizing, tracking, and archiving clinical and post-marketing regulatory dossiers.

6. Managing stakeholders across line functions and geographies. 7. Managing assigned individual projects and holding complete responsibility throughout the document/project lifecycle.

8. Ensuring consistency at all times with compulsory and voluntary codes of conduct, appropriate legislations and compliance with internal SOPs.

9. Building-up newer competencies and enhance existing competencies; analyzing skill/process gaps and bridging the gaps by developing expertise/process maps. Developing cross-functional skills in publication writing.

10. Training peers in regulatory writing.

11. Mentoring and coaching of direct reportees, if any

12. Utilizing AI-powered drafting tools to generate first-pass content for Clinical Study Reports (CSRs), Investigators Brochures (IBs), and CTD Modules (especially Modules 2.5, 2.7, and 5), ensuring outputs are always validated against source data and regulatory expectations.

13. Applying AI-based analytics to identify trends, discrepancies, and data-quality issues within clinical datasets, enabling more robust interpretation and narrative development

14. Employing AI-driven literature review, citation management, and evidence-synthesis platforms to accelerate background research, risk–benefit analyses, and safety-signal evaluations