OVERVIEW

DESCRIPTION

• Determining the schedule for projects, including deadlines, from initiation to final product, as well as the amount of time to be spent on each stage of the project and identify individuals who will be responsible for completing tasks.
• Developing a project analysis plan, including computer-generated table specifications, statistical analysis plan, and research report format and then assigning tasks and providing necessary project materials to team members
• Verifying statistical programs, statistical results, and data sets used in statistical section of technical documents and writing statistical section of technical documents, including protocols when requested.
• Specifying statistical terms and procedures and defines equations for derived variables.
• Oversee progress and development of research reports, and direct technical word processor and reviewing project status on regular basis, and prepare project summaries for weekly/monthly status meetings.
• Maintaining client contact, under the direction of the Director, Technical Analysis, according to schedule or as deemed necessary and providing final quality assurance check of research report.

REQUIREMENTS

• Education: An M.S., M.A., or M.Ph. in statistics, biostatistics, or epidemiology is required.
• Experience: A minimum of five years experience with the design and analysis of clinical trials is required. Individual must also be able to demonstrate ability to effectively manage numerous projects simultaneously and direct staff efforts in an efficient manner and have a passion for state of the art statistical applications in clinical research.

COMPENSATION