Senior Medical Writer

Role Overview:

• You will author and edit clinical and regulatory documents including protocols, investigator brochures, and clinical study reports.
• This fully remote position is based in Brazil and offers exposure to complex submission projects.

Key Responsibilities:

• Critically evaluate medical literature and interpret clinical data to produce scientifically rigorous documentation.
• Manage timelines and priorities across multiple concurrent assignments, working independently with clients.
• Provide mentorship to team members and contribute to improving writing processes.

Qualifications:

• You have at least 3 years of regulatory medical writing experience with a scientific or medical degree.
• Strong knowledge of ICH guidelines, GCP, and regulatory document structures is required.
• Exceptional written communication and project leadership skills are essential.

Benefits:

• Fully remote work with flexible schedule.
• Opportunity to work on diverse clinical development projects across pharma, biotech, and medical devices.
• Collaborative environment with mentorship opportunities and professional growth.