Statistical Programmer - Contract
Statistical Programmer -Contract
Beaufort CRO seeks an experienced Statistical Programmer for contract based work.
The Statistical Programmer's duties include SAAS 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.
Beaufort is a global CRO built around one purpose- helping life science companies improve and save lives through rapid development and commercialization of innovative products.
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, 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:
• Minimum Bachelor's degree.
• 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 offers a different CRO experience. It's not just about what we do, it's how we do it. Together our team brings a level of passion, knowledge and commitment to our projects and clients. We foster a culture of excellence specializing in in-vitro diagnostics, clinical project management, quality oversight and regulatory solutions.
At Beaufort you will be part of industry leading expertise with a shared sense of purpose and unwavering accountability to help clients achieve successful market authorization.
Beaufort is an equal opportunity employer and values diversity.
Apply Now
Beaufort CRO seeks an experienced Statistical Programmer for contract based work.
The Statistical Programmer's duties include SAAS 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.
Beaufort is a global CRO built around one purpose- helping life science companies improve and save lives through rapid development and commercialization of innovative products.
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, 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:
• Minimum Bachelor's degree.
• 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 offers a different CRO experience. It's not just about what we do, it's how we do it. Together our team brings a level of passion, knowledge and commitment to our projects and clients. We foster a culture of excellence specializing in in-vitro diagnostics, clinical project management, quality oversight and regulatory solutions.
At Beaufort you will be part of industry leading expertise with a shared sense of purpose and unwavering accountability to help clients achieve successful market authorization.
Beaufort is an equal opportunity employer and values diversity.
Apply Now