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Statistical Programmer - Contract

Remote: 
Full Remote
Experience: 
Senior (5-10 years)
Work from: 
Virginia (USA)

Offer summary

Qualifications:

Bachelor’s degree, 5+ years experience, SAS programming skills.

Key responsabilities:

  • Review and finalize statistical analysis plans
  • Create analysis datasets and perform statistical analysis
  • Provide final reports and archive documentation
Beaufort CRO logo
Beaufort CRO Research SME https://beaufortcro.com/
51 - 200 Employees
About Beaufort CRO
Beaufort is a global CRO built around one purpose — helping life science companies improve and save lives through the rapid development and commercialization of innovative products. Our shared interest and commitment to your success drives our entire organization to deliver best-in-class clinical trial services, regulatory strategy and planning, data and business analytics, data management and statistics, and quality services.We are:◈ MedTech Focused - Industry-leading expertise to streamline your clinical development.◈ IVD Specialists - Two decades of extensive diagnostic experience.◈ Results Oriented - Guided by efficient and adaptive clinical trial management. ◈ Partnership Driven - 94% of clients rate Beaufort higher than other CROsOur experience includes:◈ 500+ Regulatory Submissions including 510(k)s, PMAs, IDEs and CE-Marks◈ 4,000+ Clinical Study Sites Around the Globe◈ 1,000+ Clinical Trials Across a Wide Variety of Indications and Testing Platforms◈ 2,600+ Clinical Professionals in Over 50 CountriesSee how Beaufort CRO can accelerate your medical innovation -- and put our experience to work for you.
See more Beaufort CRO offers

Job description

 
 

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. 

 

Required profile

Experience

Level of experience: Senior (5-10 years)
Industry :
Research

Hard Skills

Clinical Data ReviewStandards OrganizationSAS MacrosStatistical AnalysisDatasetInternal DocumentationProject Planning
Are you interested?

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