Senior Biostatistician (CDS) at Labcorp Drug Development

Job Primary Functions

• Perform Lead Biostatistician role on medium complexity studies, providing statistical oversight and attending relevant project meetings
• Perform project management activities for identified projects including resource planning, timelines and milestone management
• Preparation of Statistical Analysis Plans (including mock TFL shells) for medium complexity studies under the supervision of more senior statistical staff
• Perform complex statistical analyses, quality check statistical analyses developed by other statisticians
• Conduct overall statistical review of TFLs for complex studies prior to client delivery
• Review CRF and other study specific specifications and plans
• May perform sample size calculation for simple studies under the supervision of more senior statistical staff
• Develop the statistical sections of the protocol for simple to medium complexity studies under the supervision of a statistical consultant
• Provide statistical input and review of the CSR for medium complexity studies
• Preparation and review of randomization specifications and generation of randomization schedules
• Mentor of biostatisticians within project activities; assigned tasks related to the development of staff within the department
• Present and share knowledge at team meetings and/or at monthly seminars
• Attend bid defense meetings for medium complexity studies in order to win new business
• Represent the department during project-driven client audits.

Job Qualifications

• Master’s degree, equivalent, or higher in Biostatistics or related field
• You must have some previous experience of Leading studies as a Biostatistician in either a biotech, CRO or pharma company
• Ability to program in one or more statistical software packages (SAS) used to conduct statistical analyses. SAS proficiency including use of a variety of statistical procedures e.g., non-parametric analysis, linear and non-linear models, categorical data and survival analysis
• Ability to effectively communicate statistical concepts
• A good knowledge of the overall clinical trial process
• Experience in the preparation of Statistical Analysis Plans, analysis, reporting, etc
• You must be fluent in English language (both verbal and written)