Thermo Fisher Scientific seeks a Medical Writer to develop high-quality clinical and scientific documentation for internal and external stakeholders. The role involves authoring study reports, protocols, and regulatory submissions while ensuring compliance with quality standards and contributing to program management activities.

Responsibilities

Author clinical study reports, study protocols, and data summaries as primary writer

Assist with regulatory documents including IBs, INDs, and MAAs

Ensure compliance with quality processes and document requirements

Support program management activities including timelines, budgets, and forecasts

Represent department at project meetings and coordinate with internal/external stakeholders

Requirements

- Bachelor's degree in scientific discipline or equivalent qualification
- 2+ years of experience in medical or scientific writing
- Knowledge of regulatory documentation and drug development processes
- Solid grammatical, editorial, and proofreading skills
- Ability to interpret and present complex data accurately and concisely
- Proficiency with document management systems, Excel, and Outlook
- Pharmaceutical or CRO industry experience preferred

📌 Medical Writing Editor I (India)
🏢 Thermo Fisher Scientific
📍 India