We are seeking a full-time Biostatistician for our Clinical Pharmacology Department. The selected candidates will be responsible for developing statistical analysis plan, performing statistical analyses using SAS and preparing reports for assigned projects.
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Requirements- We are looking for candidates with advanced degree in Statistics, Biostatistics or a related field and experience in pharmaceutical clinical trials.
- We prefer 3+ years industry experience
- Proficiency in SAS Programming
- The ability to organize multiple projects and excellent interpersonal skills will be an asset.
- The candidate must have a high teamwork spirit and be detail oriented.
- Excellent oral and written communication skills as well as a broad knowledge of the application of statistical methods in clinical research are required.
Responsibilities- Provide input on data collection methods and execute customized electronic database transmissions to Sponsors
- Develop statistical analysis plans for simple studies including table shells and, when appropriate, other programming plans
- Execute planned statistical analysis and summarization for simple studies (including tables, figures, and data listings) independently
- Write statistical methods and results sections of reports for assigned projects
- Review draft report for consistency and completeness
- Effectively communicate with colleagues and clients regarding timelines, deliverables, and commitments
- Perform SAS programming for various complexity of studies
- Train entry-level SAS programmers as well as provide on going department training
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