[What the role is]

Clinical evaluation of therapeutic product registration submissions

[What you will be working on]

• Evaluate clinical data submitted by pharmaceutical companies and provide technical advice on data requirements for therapeutic product registration applications.
• Develop scientific opinions and position papers on evolving regulatory approach and technical requirements.
• Represent HSA at external engagements, including meeting with sponsors, technical and advisory committees.
• Foster partnership with international regulatory authorities through collaborative review and information sharing activities.
• Serve as HSA's technical expert and front scientific discussions for workshare projects with international regulators.
• Represent HSA at international regulatory forums, contributing to development of regulatory guidelines and standards.

[What we are looking for]

A bac...