• Assistance in software requirement analysis (SAR).• Working alongside the software engineering team in developing dynamic system development models for CTMS software.• Part of the medical advisory team in evaluating the market strategy and demand.• Learning IaaS provisioning as well as trainee in cloud API development.

• Managed a multi-center Phase III clinical study that will be submitted to the US FDA.• Clinical study planning of IND in Pulmonary Arterial Hypertension (PAH) (including study design, planning, coordination, timelining and pre-marketing plan and analysis for new drug development).• Completed Phase 1 CSR and IB.• Worked on protocol design and informed consent form (ICF) reviews.• Proposed study procedures, dispensing, as well as administration of IPs.

• Business development and promotion.• Operation and maintenance of dental laser medical equipment.• Assisted co-workers with international communications.• Managed academic events and communications of the Asia-Pacific Laser Institute.• Managed company medical regulatory affairs.

• Editing and translating professional publications.• Technical communications with customers and pharmacists.

• Performed regulatory management and submissions.• Collected and managed clinical information.• Internal and external correspondence.• Researched biomedical information.• Pre-marketing analysis and protocol design (CRF and ICP).• Project leader in clinical strategy, coordination, time frame, and developed plan.

• Managed a Phase III study (new formulation and dosage) for NDA submission.• Assistance in the design of the case report form (CRF).• Assistance in labeling, packaging, and delivery of investigational medicinal product.• Reviewing and revision of the study protocol, ICF, and CRF.

• Contract CRA to Wyeth Pharmaceuticals.• Assistance in designing new drug development plan.• Managed a Phase III clinical trial (department of immunology and rheumatology).• Managed a Phase IV clinical trial (psychiatric department).• Submission of new drug for review.• Design and revision of study protocol and CRF.

• Business development, promotion, and sales.

• Atorvastatin trial in NTUH - status completed. Coordinated and monitored an international, multicenter phase IIB trial in inner cardiovascular area.• Gabapentin trial in Taipei VGH - status completed. Coordinated and monitored a local registration trial in inner neuron area.• Performed regulatory submission in inner cardiovascular area.• Assistant for registration and monitored a listing trial.

• Performed cardiectomy on rats.• Surgical operations and experimentation on the usage of neutrophil elastase inhibitors.• Performed artificial heart implantation on calves.• Receptionist for visiting speakers on behalf of the Surgical Association of R.O.C. as well as Medical and Surgical Laser Association of R.O.C.