Design and evaluate oncology clinical trial frameworks — including study protocols, patient enrollment strategies, and regulatory compliance considerations
Assist in day-to-day production activities as per SOPs. Conduct basic chemical handling, mixing, and batch processing.
Monitor production processes and record process parameters.
Hands-on experience in XRD, DSC, TGA, Microscopy, Zetasizer and PSA; Responsible for day-to-day laboratory activities and team leadership; Experience in GMP-compliant laboratories and QMS.
Successful candidates will have a strong record of scientific achievement, clear intellectual drive to advance scientific understanding, and a commitment to engage collaboratively with a diverse community of scholars and transcend traditional disciplinary boundaries.
Cross-Functional Collaboration: Work closely with Regulatory, International Export, Marketing, and R&D teams to streamline the flow of information and ensure project alignment.