Description
We are seeking a Medical Writer to join our team. As a Medical Writer, you will be responsible for creating clinical trial-related documents, including study protocols, reports, and regulatory submissions.
Responsibilities:
- Create clinical trial-related documents, such as study protocols, reports, and regulatory submissions
- Develop global trial protocols that meet Japanese requirements
- Prepare post-marketing surveillance-related documents, such as safety periodic reports and re-examination application materials
- Create clinical study reports and papers
- Perform quality control on various documents
Requirements:
- Medical writing experience (not just translation)
- Bachelor's or master's degree in a scientific field
- Basic knowledge of pharmacology and medicine
- Understanding of pharmaceutical development, GCP, ICH guidelines, and domestic pharmaceutical regulations
- English reading and writing skills (able to proofread and translate English documents with a dictionary)
- Fluency in Japanese
Preferred qualifications:
- Knowledge and experience in non-clinical (pharmacology, toxicology, ADME) or clinical pharmacology
Benefits:
- Competitive salary
- Comprehensive benefits package, including social insurance and IQVIA-specific programs
- Flexible working hours and remote work options
- Opportunities for professional growth and development