Description
- § Provides statistical consulting to RMS clinical teams in design of clinical studies (including sample size estimation, power calculation and study conduct) and in the analysis and interpretation of study data. Works on complex statistical problems in which analysis of data requires an in-depth evaluation of various factors.
- § Provides statistical methodology section for study protocol, develops statistical analysis plan, performs statistical analysis and drafts statistical report as required. Provide input into clinical study reports. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results.
- § Develops systematic documentation of methods, results and statistical programming. Statistical programming may include creation of analysis specified in statistical analysis plan and ad-hoc analysis as requested.
- § Coordinates the quality-control checking of deliverables (reports, summary tables, and graphs). Independently QC the statistical outputs generated by the study programmer.
- § Participates in project team meetings independently, provides statistical expertise to the team and reports meeting discussions/decisions back to supervisor.
- § Manages multiple studies in a team and makes sure of consistencies across all studies if they are in a life cycle team. Manages timelines across all studies. Facilitates and manages workload when CROs are involved.
Education:
Minimum (required): Master's degree in Biostatistics or Statistics
Preferred: Ph.D. in Biostatistics or Statistics
Knowledge:
A thorough knowledge of experimental design, general linear model, categorical data analysis and statistical computing. Familiarity with survival time analysis and nonlinear models is a plus.
To find out more about Real please visit www.realstaffing.com