Eric Chen Quin Lam Email & Phone Number

United States

• Provides statistical consulting to clients in the biotech/pharmaceutical industry in their drug development programs with a focus on comprehensive data analysis strategies of clinical development, protocol/study.
• Statistical lead for clinical studies - consults on power/sample size calculations, design of statistical aspects of study protocols, develops statistical analysis plans, design of data capture methods, executes on.
• Leads team of statisticians in supporting and executing clinical projects.
• Hires, trains, mentors, and evaluates performance of direct reports.

• Leads team of statisticians within Data Analytics in providing data management and statistical support for claims-related research (RWD).
• Leads Data Analytics Clinical Research team in supporting and executing clinical studies for industry-sponsored and government-funded research.
• Provides scientific and operational oversight for research projects, as well as strategic input and support for business development.

• Lead statistician for industry-sponsored clinical research projects.
• Provide statistical expertise for study design of clinical trial protocols.
• Write statistical analysis plans ensuring appropriate regulatory requirements and study objectives defined in the study protocol are followed.
• Review CRFs to ensure consistency with protocol and adequacy in collecting data to meet objectives and statistical analyses defined in the protocol.
• Perform statistical analyses defined in the SAP and any post-hoc analyses and relevant exploratory analyses of clinical trial data.

Indianapolis, Indiana, US

• Statistician supporting global early phase clinical trials.
• Represent statistics function in regular meetings and collaborations with cross functional teams for compound-level clinical development plans. Key role in development and review of study design/protocol, statistical.
• Responsible for study-level statistical deliverables ensuring timeliness and quality of data management, analysis datasets and statistical output.
• Lead statistician for early phase and biopharmaceutics trials for global regulatory submissions of new drug approvals.

• Lead a 6-member team in data compilation, programming, data analysis, statistical modelling and report writing.
• Regular presentations of key results and trends to management and external key stakeholders.

Doctor Of Philosophy (Phd), Statistics

Bachelor’S Degree, Economics And Statistics (Honours In Statistics)