Offer summary
Qualifications:
Bachelor’s/Master’s degree in biomedical or life sciences, Minimum 2 years of industry experience, Knowledge of global regulations (FDA, ICH), Understanding of electronic Common Technical Document (eCTD) requirements.
Key responsabilities:
- Write, edit, review clinical documentation
- Track and collect documents for CSR appendices
- Perform quality control reviews of documents
- Collaborate with teams on patient safety narratives
- Act as a backup contact for project managers