Simon P. Email & Phone Number

Cincinnati, OH, US

• Lead statistical and programming activities for assigned projects and train new analysts
• Contribute to clinical development plan preparation
• Develop Data Analysis Plans for assigned projects
• Review study protocols and identify appropriate statistical methodologies
• Program study analyses, review study results, and prepare statistical methods sections for clinical/statistical reports
• Communicate project requirements for CRF design, database design, and database cleanup to ensure that key study variables are suitable for analysis

Bryan, TX, US

• With the designated emphasis in biostatistics, Oncology
• Designed experiments, analyzed data, and interpreted results of oncology preclinical studies. Determined appropriate statistical method for longitudinal repeated measures data. Applying the mixed-effect model in R..
• Developed protocol of innovative method for bone functionality change analysis.
• Independently implemented newly developed complex statistical methods in R without a commercially available software package. It is the first time implementing quantile functional regression on quantlets in the field..
• Developing R package for the method (under progress)
• Built and maintain three different RStudio Server for efficient lab work.

• Data analysis based on statistical analysis plan using SAS and R under SDTM, and ADaM standards.
• Communicate effectively with the medical team to design an analysis plan
• Communicate effectively with the data management team and program team to analyze data and interprets results from clinical trials
• Work with the data management team and program team to support PK/PD analysis.

College Station, TX, US

Dept. of Statistics

Dallas, TX, US

Rahway, New Jersey, US

• Served as data project lead (MK-3475-028) of teams across GDOs in Japan, and China. Successfully achieved study milestones and ensured accuracy of data.
• Involved in developing protocols and data review plans.
• Participated in database design meetings.
• Evaluates appropriateness of available eCRF, report, and queries and ascertains needs for potential program development of new ones.
• Gained good knowledge of data mappings, Coding, Web-based Randomization, CDASH, CDR, CDISC, SDTM, and ADaM standards.
• Interacted efficiently, coordinated, and worked closely with people across functional areas.

Rahway, New Jersey, US

• SAE reconciliation; ensure that all activities are conducted in compliance with relevant regulatory requirements.
• Gained good knowledge of ICH-GCP.

北京, Beijing, CN

• Small molecular screening for analgesic effect in preclinical development

Molecular cytological and safety evaluation laboratory (simultaneously). My work is mainly about new drug testing by using pharmacological, molecular cytological, pathological, toxicologic and physiological methods. I was working in molecular cytological lab and in charge of safety evaluation lab.

Doctor Of Philosophy - Ph.D., Biostatistics

Master Of Science - Ms, Statistics

Bachelor Of Applied Science (Basc), Biomedicine