Biostatistician I
As a Biostatistician at Rho, you will participate in multiple clinical trial project teams. Communicating statistical issues as they arise to Rho team members as well as maintaining a steady, open dialogue with study team members regarding study execution as it relates to timelines, data quality, and interpretation of the results. Rho's environment is team-oriented. Good communication skills and the ability to work with a team are crucial for success. Rho's high quality standards require careful attention to accuracy and details
Responsibilities
Under the direction of a lead biostatistician, you will:
- Develop, test, maintain, and archive SAS program code to conduct planned and exploratory statistical analysis of clinical data
- Interpret the results using written, oral, and graphic methods, as appropriate, either in a statistical report or as part of a clinical trial report
- Develop CDISC compliant datasets
- Prepare analysis plans and specifications for analysis data sets and data displays (tables, listings, & graphs)
- Collaborate with statistical programming team on the production of datasets and displays
- Identify and troubleshoot missing, miscoded, or incomplete data and work with clinical team to resolve issues
- May perform sample size computations in conjunction with clinical staff to determine the appropriate number of subjects necessary for the investigation, taking into consideration the interpretability of the results from a statistical and clinical perspective as well as applicable regulatory requirements
- May develop and/or validate randomization schemes for clinical trials
Qualifications
- Master's degree in biostatistics, statistics, or a related field is required
- 0-2 years of experience working in a CRO in the pharma/biotech industry
- Good understanding of basic statistical procedures and methodology is required along with strong SAS programming skills
- Excellent organizational skills, written and verbal communication skills, and working knowledge of Microsoft Office Suite is a must
- Ability to work on several projects simultaneously and manage deadlines
- Familiarity with CDISC standards is a strong plus.
Rho is a full-service contract research organization optimally sized to deliver results from clinical research with agility and adaptability. Maximizing profitability, stability, and planned growth has helped provide us with the experience, capacities, and capabilities of a larger organization—all without losing touch with our entrepreneurial passion.
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Because Rho recognizes great people are our most important asset, we attract and retain the best and brightest.