Responsibilities

• Draft and edit medical documents, including clinical study reports, regulatory submissions, and publication materials.
• Collaborate with researchers, clinicians, and other stakeholders to gather and interpret scientific data.
• Ensure compliance with regulatory requirements and company standards in all written materials.
• Maintain up-to-date knowledge of medical terminology and writing conventions.
• Participate in team meetings and contribute to project planning and timelines.
• Review and provide feedback on documents produced by other writers.

Requirements

• Bachelor's degree in a relevant field such as life sciences, communications, or medical writing.
• Strong writing and editing skills with attention to detail.
• Ability to understand and synthesize complex scientific information.
• Proficiency in Microsoft Office Suite and familiarity with reference management software.
• Excellent organizational and time management skills.
• Strong interpersonal skills and ability to work collaboratively in a team environment.

Benefits

• Competitive salary and performance-based bonuses.
• Comprehensive health, dental, and vision insurance plans.
• 401(k) retirement plan with company matching.
• Flexible working hours and opportunities for remote work.
• Access to ongoing training and professional development programs.
• A supportive and inclusive work culture focused on career advancement.