- Manages and oversees clinical development program taskforce, which includes preclinical, CMC, regulatory and medical, to build strategies towards NDA filing with the US FDA with consideration of budgets, requirements and timelines- Manages Medical Affairs department to build strategies towards alignment with corporate objectives and performs risk assessments - Manages clinical projects from vendor selection, trial start up, conduct, analysis to clinical study report.

• Managed clinical study operations for Industry-sponsored and Investigator-initiated trials, including project timelines, quality of deliverables, and managing trial budget(s)• Oversight of CRO and vendors • Represented Clinical Operations in cross-functional initiatives• Coordinated internal and external pre-clinical and clinical development activities

• Contributed to the development, planning and collaboration with internal and external stakeholders to deliver accurate patient and site operations plans and budget for regional (including Japan) and global studies during request for proposal, bid defence meeting, early engagement and engagement after study award• Managed delivery of patient and site operations plans for regional and global studies, including vendor contracting, engagement and oversight, presentation during Investigators’ Meeting and accompanied site visits with CRA during monitoring visit or booster visit• Managed a program in Malaysia with Sponsor’s Medical Affairs team which involves program oversight and management, budget and milestone planning, risk management as well as revenue recognition• Initiated and lead process improvement of innovative patient recruitment and retention strategies• Acted as central contact for clinical team and Sponsor for designated project communications and correspondences• Managed new hire and mentored interns

• Site Management with focus therapeutic areas on oncology and hematology studies as well as cardiology studies • Performed clinical monitoring aspect and project management aspect of designated projects in accordance with Amgen's SOP• Experienced in start-up activities, clinical on-site activities (source data verification, drug accountability) as well as on-site termination activities (drug return/destrcution, archival of site files)• Perform regulatory and ethics committee submissions

• Site Management with focus therapeutic areas on oncology studies and epidemiology studies in Singapore and Malaysia• Performed clinical monitoring aspect and project management aspect of designated projects in accordance with both PAREXEL and sponsor's SOP• Experienced in start-up activities, clinical on-site activities (source data verification, drug accountability) as well as on-site termination activities (drug return/destrcution, archival of site files)• Perform regulatory and ethics committee submissions for Singapore and Malaysia studies• Perform qualification, initiation, monitoring and termination of investigational sites• Experienced in handling sponsor audit both in sponsor office and on site

• Provided assistance to various Clinical Operations Leaders to manage projects in the APAC region including Singapore, Malaysia, Taiwan, Korea, Hong Kong and Philippines• Collaborated extensively with an international project team• Compiled site regulatory documents and perform quality check prior to submission to client• Maintained both paper and electronic Central Files by ensuring proper and timely collection of documents and ensured it is client-ready• Maintained internal and client's trackers for various activities including, IRB/EC submission, safety reporting and communication with the sites, during maintenance phase of study• Reviewed and analyzed reports generated from Clinical Trial Management System (CTMS)• Trained newly hired Project Assistant to analyze reports and maintain trackers. • Acquired knowledge on site management, ICH-GCP, local regulations of APAC countries and project management and planning

• Conducted a full independent research in the field of Biochemical and Molecular Pharmacology• Acquired skills in human cell cultures, genomics and proteomics related techniques, drug uptake assays as well as handling of radioactive materials• Developed effective interpersonal, communication and presentation skills

• Accepted into the Undergraduate Research Opportunity Programme in Science• Conducted a full independent research in X-ray crystallography and structural biology• Acquired skills in bioinformatics, molecular cloning, protein purification and bacterial cell cultures