Job Summary

The Executive – Regulatory & Scientific Affairs will support scientific, clinical, and regulatory activities associated with pharmaceutical product development and lifecycle management. The role involves conducting comprehensive literature reviews, preparing clinical and non-clinical regulatory documents, supporting regulatory submissions, and contributing to scientific evaluations in accordance with global regulatory requirements.

Key Responsibilities

Scientific and Literature Research

• Conduct comprehensive literature searches using scientific databases such as PubMed, Embase, Cochrane Library, and regulatory agency databases.
• Perform secondary research to gather scientific, clinical, toxicological, and regulatory information from journals, publications, public databases, and health authority resources.
• Evaluate and summarize scientific evidence to support product development and regulatory sub...