Offer summary
Qualifications:
Bachelor's/Master's degree in biomedical or life sciences, Minimum 2 years of clinical documentation experience, Prior experience in pharmaceutical or biotechnology, Knowledge of FDA, ICH guidelines, Familiarity with eCTD requirements.
Key responsabilities:
- Write, edit, and review essential documents.
- Track clinical study report patient safety narratives.
- Collect and support documents for CSR appendices.
- Assess data from clinical studies.
- Perform quality control reviews of documentation.