Duties: Perform tasks under the guidance of project lead or CMS departmental principals on analytic design and statistical analytic planning, coordinate real world database management, and data warehouse construction or maintenance. Develop documentations of analytic plans, prepare for statistical concept communications and be able to advise on analytic strategies and recommend methodological solutions on complex analytic topics. Lead and perform statistical analyses, modeling, reporting, analytic interpretations, and slide development. Develop SAS macro libraries to standardize disease identification, cohort constructions, mapping of healthcare resource utilization and expenditures to standard metrics for product value propositions
Requirements: Software Developer, Software programmer, Data Analyst/Scientist

Duties: Lead complex clinical trials or indication corresponding to one or several compounds in development; Represents Biostatistics as a member of cross functional teams, accountable for statistical aspects of statistical design, study setup, execution, analysis and reporting of clinicals; Manage the timelines and oversee the quality of statistical analyses by CRO or internal teams; Undertake new and highly complex issues requiring advanced analytical thought with minimal supervision; Support global submission deliverables as needed including responses to health authority queries, advisory committee meeting preparation, etc; Provide statistical support for the Biometrics Department’s infrastructure needs
Requirements: MS in Statistics/Biostatistics and at least 10 years of relevant pharmaceutical experience or a PhD in Statistics/Biostatistics with more than 6 years of’ relavant pharmaceutical experience; Knowledge of pharmaceutical environment and regulatory requirements; Comprehensive knowledge and understanding of advanced statistical concepts and techniques applicable to Clinical Research

Duties: Lead one or several indications corresponding to one or several compounds in development; Represents Biostatistics as a member of cross functional teams, accountable for statistical aspects of clinical development plans, studies, submission activities and regulatory interactions; Manage the timelines and oversee the quality of statistical analyses by CRO or internal teams; Lead or contribute to statistical innovation activities including innovative design, advanced analytics, data visualization and template development
Requirements: A Ph.D in Statistics or Biostatistics with more than 10 years of pharmaceutical experience; Strong knowledge of pharmaceutical environment and broad experience with multi-phase development; Strong knowledge and in-depth understanding of advanced statistical concepts and techniques applicable to Clinical Research