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Sas Programming Consultants Jobs (NOW HIRING)

Skilled SAS programming knowledge. * Demonstration of innovation by development or novel ... Developing consultation skills that include design, and data management issues for clinical and non ...

... strategic consulting and global leadership management approach. Our solutions are designed ... This person will bring strong SAS programming experience and a practical understanding of ...

... strategic consulting and global leadership management approach. Our solutions are designed ... This person will bring strong SAS programming experience and a practical understanding of ...

... consultation with superiors as appropriate. Analyst will determine if the request requires a new ... focus SAS Skill Competencies: Accessing Data Creating Data Structures Managing Data Generating ...

Senior Statistical Programmer/Analyst Consultant (Cardiovascular, Renal) United States Are you ... Strong SAS programming experience within the pharmaceutical/CRO industry * Hands-on experience ...

... consulting including: * 5 years of experience in a leadership role with 2 years in a formal ... Experience with SAS systems or SAS programming. #LI-CC World-class benefits Highlights include.

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As of Sep 14, 2026, the average hourly pay for sas programming consultants in the United States is $49.00, according to ZipRecruiter salary data. Most workers in this role earn between $34.38 and $61.54 per hour, depending on experience, location, and employer.

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Infographic showing various Sas Programming Consultants job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 81% Full Time, 13% Part Time, 4% Contract, and 1% Nights. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $101,929 per year, or $49 per hour.

Biostatistician

Emeryville, CA โ€ข On-site

Crowdstaffing
11 - 50 employees

Contractor

Re-posted yesterday


Job description

Company Description

Crowd Staffing

Job Description


Minimum Qualifications

Education:

Master's degree in Statistics or Biostatistics with at least two years related experience

Skills:Required

  • PHARMACEUTICAL FDA
  • SAS
  • STATISTICAL ANALYSIS
  • BIOSTATISTICS
  • Minimum 2 years experience in BIostats role within Pharamceutiocal or Diagnostics industry.
  • Minimum 2 years Manufacturing and product development Pharmaceutical/Biotechnology industry experience (assay validation, product specification setting, OOS, SPC, process optimization, etc.).
  • Minimum 2 years experience managing people in a Biostats or clinical capacity.
  • Demonstrated sound knowledge of statistical applications to clinical and nonclinical projects. Demonstrated technical expertise across a range of commonly used statistical methodology.
  • Knowledge of appropriate regulations and guidance documents. Broad experience across a range of clinical and nonclinical projects and demonstrated support of diverse client needs.
  • Demonstrated management and leadership skills.
  • Skilled SAS programming knowledge.
  • Demonstration of innovation by development or novel application of statistical methods.
  • Sound knowledge of theoretical statistics and statistical applications
  • Must have proficiency as an SAS programmer
  • Knowledge of FDA regulations and guidelines is a plus.
  • Good communication and presentation skills.
  • Ability to work effectively in both in a team environment and independently.
  • Ability to work on several projects simultaneously.
  • Possess good problem solving skills.
  • Self-motivated
  • Capable of addressing unique problems
  • Experience in the diagnostics area is preferred.

*

  • Developing consultation skills that include design, and data management issues for clinical and nonclinical projects.
  • Work with project teams to produce protocols, analysis plans and final reports for clinical and nonclinical projects.
  • Plan, coordinate and produce statistical analyses, summaries and write formal memoranda.
  • Produce SAS programming and other software package programming to analyze data.
  • Interpret the project implications of regulatory guidelines. Interact with FDA, other regulatory or auditing agencies as appropriate in statistical aspects of study design, data analysis, and justification of statistical procedures.
  • Represent Biostatistics on company-wide project teams. Serve as primary liaison between Biostatistics and key internal clients with regard to resource needs and timelines.
  • If appropriate, interact with counterparts at companies collaborating with other Teams including proactively engaging with joint development corporate partners.
  • Initiate methodological research in statistics to improve biostatistics methodology used in development products consistent with corporate priorities and timelines.
  • Develop Clinical and Nonclinical Biostatistics procedures and guidelines to comply with corporate policies and procedures.
Additional Information

All your information will be kept confidential according to EEO guidelines.