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Job Requirements of Statistical Programmer - Contract:
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Employment Type:
Full-Time
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Location:
Virginia Beach, VA (Onsite)
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Statistical Programmer - Contract
Beaufort CRO seeks an experienced Statistical Programmer for contract-based work.
The Statistical Programmer’s duties include SAS programming and analysis for one or more particular life science client projects, including clinical trial studies within the in-vitro diagnostic (IVD), medical device, and pharmaceutical industry.
Key responsibilities include:
- Review of pre-project and planning activities such as: Protocol and Case Report Form (CRF) Review, Statistical Analysis Plan Review, Programming Plan (including analysis dataset specifications).
- Once the plan is approved and output finalized, the Statistical Programmer creates the analysis dataset and performs statistical analysis according to the plan. Validates the statistical analysis according to the plan. Incorporates client changes or modifications as required. Provides documentation logs to include in the project/study files.
- Finalizes statistical analysis and provides final report for inclusion in the Clinical Study Report (CSR) and all appropriate project documentation. This includes tables, listings, and figures. Archives all documentation.
- Perform other project-related tasks assigned to the Statistical Programmer role as specified in the individual’s Statement of Work.
Qualifications:
- 5+ years of experience
Top 3 skills needed to perform the work requested:
- SAS programming skills
- Knowledge of industry standards
- Understanding of clinical trial data, preferably clinical trial data for in vitro diagnostic trials.
Non-technical/personal skills needed:
- Effective communication both verbal and written
- Collaborative work style
Beaufort is an equal opportunity employer and values diversity.
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Recommended Skills
- Biology
- Case Report Forms
- Clinical Study Reports
- Clinical Trials
- Communication
- Pharmaceuticals
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