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Biostatistician

Research Triangle Park, NC

Posted: 09/07/2018 Job Category: Clinical: Biometrics Job Number: 2130

Our Biostatisticians applies knowledge of statistics to independently provide statistical consulting, assist with study design and protocol development, performs statistical analysis of clinical trials. They will also review project related documents, prepare statistical analysis plans (SAPs) and statistical reports. This individual will develop analysis data specifications, create analysis datasets, Tables, Listings and Graphs (TLG) of clinical trial data using SAS. He or she will also perform quality control of TLGs and derived data sets created by others. Develop and validate SAS programs, micros, and utility tools. Apply advanced programming knowledge to support programming efficiencies.

Responsibilities:
  • Drafting (with supervision) statistical sections of protocols, performing sample size and power calculation for studies, and creating randomization schedule per study design and relevant specifications
  • Reviewing case report forms (CRFs), data management plans, data specifications and other related study documents
  • Drafting (with supervision) statistical analysis plans (SAP) in accordance with the protocols and SAS programs to develop statistical models and complete statistical analyses
  • Supporting integrated summaries of safety and efficacy (ISS and ISE) for regulatory submissions
  • Drafting (with supervision) analysis data specifications
  • Developing SAS programs to create derived variables and analysis data sets and computer programs to generate listings, tables, and graphs using SAS
  • You' ll also be Responsible for:
  • Performing quality control of analysis data and TLGs
  • Reviewing, providing input and interpreting of analysis result to clinical study report


Qualifications:
  • Advanced degree (MS or PhD, or equivalent) in statistics or closely related field
  • 2-4 years direct advance knowledge of clinical trials design and analysis experience with advanced SAS programming experience
  • Working knowledge of CDISC standards and application of those standards to projects
  • Ability to effectively communicate with others on the project team and in the department; strong interpersonal communication skills
  • Detail oriented, well organized
  • Ability to work on several projects simultaneously
  • Demonstrated knowledge of design of clinical trials and regulatory requirements
  • Demonstrated working knowledge of advanced SAS macro development and code generation/management algorithms
  • Knowledge of design of clinical trials and regulatory requirements
  • Excellent English communication skills (verbal, written & interpersonal)

Demeika Roberts

Demeika is known for her enthusiasm in working closely with hiring managers to assess their needs, creatively solve problems, and passionately help candidates find their “perfect fit” dream jobs.

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