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SAS Programmer Data Analyst


Science. Technology. Service.

Bracket innovates at the leading-edge of clinical research data, one exceptional service at a time. From the advanced technology of our eCOA electronic Clinical Outcomes Assessments flexible platform, to the efficiency of our scalable and configurable Randomization and Trial Supply Management (RTSM) Clinical IRT solution, to our science-focused Rater Training and Quality Assurance programs, Bracket does it faster, better and with an eye on the future of our industry. To achieve this, we maintain an unwavering commitment to employing only the brightest, most talented colleagues gleaned from a wide variety of professional fields. If you are a creative problem-solver and have a hard-wired, instinctual commitment to exceptional customer service, we'd love to talk to you! 

Bracket is looking for a Clinical Data Analyst with SAS programming experience to support the implementation and maintenance of Bracket’s products and services to meet customer’s needs. The Clinical Data Analyst will author requirements and programs for data extracts, listings and summaries as needed to support the study team (both internal and external) needs during requirement, implementation and maintenance phases of a project. The Clinical Data Analyst will provide intra department validation, unit testing and code review with peers. The Clinical Data Analyst will provide consultation to internal teams to advance the implementation of best practices and standards.

Essential Duties and Responsibilities:

  • Author specifications, programming and maintain code used for data management & validation, ad-hoc reports, data exports, program validation and analytics.
  • Assists internal and external customers such as Project Management, Study Architect, Testing, Data Management, Clinical teams and Biostatistics functions with the intent of process efficiencies and improvement
  • Communicates effectively within a multi-disciplinary project team to complete assigned tasks on time and within budget.
  • Evaluate potential software solutions.
  • Performs all work in accordance with documented Standard Operating Procedures (SOPs), Working Instructions and Best Practices.
  • Assists in developing and improving Standard Operating Procedures (SOPs), Working Instructions and Best Practices.
  • Adheres to Good Clinical Practices (GCP), 21 CFR Part 11 and other regulatory requirements as required.
  • Assist with other departmental initiatives and projects as required.

Education and Experience 

 Degree in Computer Science, Math, Biostatistics, or similar OR working experience.

  • 3-5 years’ experience SAS/BASE experience, preferable in a CRO/pharma programming. 
  • Proficiency in SAS/BASE, SAS/CONNECT, SAS ODS, SAS macros with SAS/GRAPH and SAS/STAT as a plus.
  • Proficiency in MS Excel, Microsoft SQL Server 2008 R2 and Microsoft Visual Studio, and SQL a plus.  
  • Strong knowledge of relational data base structures and experience working with complex data systems,
  • Knowledge of industry guidance and standards for data collection and tabulation such as CDASH and CDISC SDTM.
  • Degree in Computer Science, Math, Biostatistics, or similar OR working experience.
  • Exhibits an entrepreneurial spirit while working within the industry regulations and guidance.
  • Ability to communicate effectively, both verbal and written.

We offer a highly competitive base salary and an outstanding benefits program, including medical, prescription drug, dental, vision, 401(k) with Company match, life insurance, and generous paid time off.

We are an Equal Opportunity Employer, M/F/D/V




















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