Associate Medical Writer

📋 Description

• Support study startup activities by preparing, organizing, and maintaining study-specific medical
• Review clinical study protocols and imaging requirements to understand study procedures, schedules
• Create, update, review, and finalize study documentation, including site manuals, supporting forms
• Prepare and maintain Notes to File, protocol amendment impact assessments, correction records, and
• Develop and maintain source documents and electronic clinical forms to support study execution and
• Prepare agendas, meeting minutes, and action item records for study startup, project meetings, and

🎯 Requirements

• Bachelor’s degree in Life Sciences, Biological Sciences, Physical Sciences, Pharmacy, Healthcare
• At least 1 year of medical writing experience is preferred. Equivalent experience in clinical
• At least 2 years of experience in pharmaceutical, biotechnology, clinical research, healthcare
• Understanding of medical writing, scientific documentation, clinical research principles, and
• Knowledge of clinical trial terminology, clinical research processes, and medical imaging concepts
• Strong working knowledge of Microsoft Office applications, including Word, Excel, PowerPoint, and

🎁 Benefits

• Competitive compensation and incentive opportunities.
• Provident fund benefits.
• Medical insurance coverage.
• Remote work flexibility and access to modern office facilities.
• Employee engagement programs and local events.
• Professional development opportunities and potential for long-term career growth.