• 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 design, regulatory submission strategies, regulatory communication.• 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 statistical analysis and programming, reviews and presents study results to key stakeholders. • 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.

• 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 analysis plan, clinical study report and regulatory documents. • 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.