Description
Key Responsibilities:- Work with Pharma Comapny and contract research organization (CRO) staff to assemble, curate, and quality check raw and derived clinical trial datasets
- Conduct statistical analyses of laboratory, pharmacodynamic, and phenotypic data
- Produce tables, graphs, and visualizations for internal and external presentations
- Develop and run a statistical codebase in conjunction with Pharmaceutical Company and CRO staff
- Assist with analyses and visualization of pre-clinical research data
Qualifications:
The ideal candidate will have a Bachelors in a quantitative science and a MS in (Bio)statistics, with the ability to apply correct theoretical statistical methods in clinical trial applications. A minimum of 5 years' experience is required, ideally in a biopharmaceutical or CRO setting, although experience in an academic research setting will also be considered. In addition, the candidate will have:
- Demonstrated proficiency in both SAS and R programming languages
- Demonstrated proficiency in Microsoft Excel and Powerpoint
- Experience with data extraction, manipulation, and analysis, preferably in the early-stage clinical trial setting
- Experience with perl and/or other scripting languages, and comfort working in Linux and Windows environments
- Demonstrated ability to work independently
- Excellent verbal and written communication skills with the ability to convey ideas and methods in a clear and succinct manner understandable to non-statisticians
- Superior presentation skills, and the proven ability to work in a team setting
To find out more about Real Staffing please visit www.realstaffing.com