Duties: Serve as a statistical consultant for other members of the department and staff members from other Biostatistics departments within the company. Maintain knowledge and awareness of developments in Biostatistics and clinical trial methodology, and regulatory requirements that impact analyses. Represent clients at meetings with regulatory agencies or other regulatory meetings, may participate as a member of a Data and Safety Monitoring Committee. May participate in independent research activities, teaching opportunities, presentations, and preparation of manuscripts for publication, as approved. May participate as high level lead biostatistician on major project(s) including developing/reviewing protocols, preparing analysis plans, and writing sections of joint clinical/statistical reports, integrated summaries and/or new drug application (NDA) sections, as required. Provide advanced technical expertise for internal and external clients. Assist and contribute to governance structures whe...
Requirements: Bachelor's Degree Biostatistics or related field and 12 years relevant experience including 6 years experience managing staff Req Or; Master's Degree Biostatistics or related field and 12 years relevant experience including 6 years experience managing staff; Typically requires 12+ years relevant experience including 6 years experience managing staff or Equivalent combination of education, training and experience

Duties: Provide experienced technical expertise to develop process methodology for department to meet internal and external clients’ needs. Plan and coordinate the development of integrated programming solutions serving the full spectrum of statistical programming needs. Provide technical expertise and leadership to the department. Provide internal consulting services, including specifications and user needs analysis for complex project or client requirements
Requirements: Master's/Bachelor's Degree in Life Science/Computer science/Engineering/Statistics/Biostatistics with Min 8+ Years Exp in clinical SAS Programing with hands on SDTM&ADAM/TFL is mandatory; Equivalent combination of education, training and experience in lieu of degree Req; Knowledge of statistics, programming and/or clinical drug development process; Advanced knowledge of computing applications such as Base SAS, SAS Graph and SAS Macro Language

Duties: As a Senior Statistical Programmer, you will be given access to cutting-edge, in-house technology and opportunities to work on global projects across a variety of therapeutic areas. You will plan and coordinate the development of integrated programming solutions, serving the full spectrum of statistical programming needs, along with providing technical expertise and leadership to the department and provide internal consulting services, including specifications and user needs analysis for complex project or client requirements
Requirements: Bachelors or Masters’ in Computer Science, Mathematics or equivalent; 5+ years Statistical Programming experience within the Life-Science industry; Experience in SAS® Base, and good knowledge of SAS® graph and SAS® Macros; Excellent knowledge of CDISC standards (SDTM and ADaM); Excellent application development skills

Duties: Develop statistical methods sections of protocols and review case report forms (CRFs). Prepare analysis plans and write specifications for analysis files, tables, and figures. Communicate with clients regarding study protocol or statistical analysis issues as they arise. Communicate with study team members regarding study execution as it relates to timelines, data quality, and interpretation of results. Interpret analyses and write statistical sections of study reports. Accountable for controlling costs and maximizing revenue recognition. Provide training, guidance and mentorship to lower level and new staff
Requirements: Bachelor's Degree Biostatistics or related field and 3 - 5 years relevant experience Req Or Master's Degree Biostatistics or related field and 3-5 years relevant experience Req Or Ph.D. Biostatistics or related field and 1 year relevant experience Req; Typically requires 3-5 years of prior relevant experience, or equivalent combination of education, training and experience; Requires advanced knowledge of job area, and broad knowledge of a other related job areas, typically obtained through advanced education combined with experience

Duties: Manage a team of Statistical Programming (SP) staff, including hiring, training, and supervising department members. Develop, recommend, and implement standard procedures, measures of performance, and training programs. Organize and allocate resources according to multi-project requirements and deadlines. Serve as lead statistical programmer on projects
Requirements: Master's Degree Computer science or related field and 5 years relevant experience including 1 year in a leadership capacity Req Or; Bachelor's Degree Computer science or related field and 6 years relevant experience including 1 year in a leadership capacity Req; Equivalent combination of education, training and experience in lieu of degree Req; Advanced knowledge of SAS and technical database skills