For companies:
For professionals:
For everyone:
For developers:
Responsibilities
Responsibilities:
- Write safety documents and patient CSR narratives for regulatory submissions.
- Work directly with global clients.
- Handle revisions, feedback, and deliver high-quality documents.
- Ensure compliance with ICH and regulatory guidelines.
Experience and Skills:
- 3+ years in medical, narrative, or safety writing.
- Strong experience in CSR narratives. Oncology experience is a big plus.
- Solid understanding of clinical research and drug development.
- Excellent English writing skills.
- Proficient in MS Word and document tools.
- Detail-oriented, organized, and client-ready.
Education:
- Bachelor's in any form of Medicine or Master's in Life sciences.
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