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 Pub Med, 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 submissions.
Regulatory Writing and Documentation