Medical Writer

Thermo Fisher Scientific seeks a Medical Writer to produce high-quality scientific documentation for clinical and regulatory purposes. The role involves authoring study reports, protocols, and regulatory submissions while collaborating with internal and external stakeholders in a remote setting based in India.

Responsibilities

• Author clinical study reports, study protocols, and related regulatory documentation
• Summarize and interpret data from clinical studies for various audiences
• Assist with complex documents including Investigator Brochures, INDs, and Marketing Authorization Applications
• Ensure compliance with quality processes and best practices for assigned deliverables
• Participate in project meetings and represent the department at key review sessions

Requirements

• Bachelor's degree in scientific discipline or equivalent qualification
• 3+ years of experience in medical writing or related scientific role
• Pharmaceutical or CRO industry experience preferred
• Strong medical writing, editorial, and proofreading skills
• Knowledge of regulatory documentation and drug development processes
• Proficiency with document management systems and Microsoft Office applications
• Ability to interpret and present complex data accurately and concisely