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Remote Clinical Sas Programmer Jobs in Arizona (NOW HIRING)

YO AI Labs

Biostatistician Expert - Remote

Phoenix, AZ · Remote

$60 - $70/hr

Analyze and validate clinical trial data. * Review and interpret Statistical Analysis Plans (SAPs ... Perform statistical analyses using SAS and/or R . * Collaborate with cross-functional teams and ...

Arsenault Inc

Data Analyst (REMOTE)

Phoenix, AZ · Remote

$115K - $126K/yr

Utilizes programming and analytical tools, including open source programs including Python, R and SAS, SQL, Oracle, or similar relational database tools to formulate models and/or extract insights.

Roche

Clinical Development Lead

Tucson, AZ · On-site +1

$100K - $186K/yr

... biomedical engineering, biostatistics/epidemiology, or a related clinical research field. * You ... This position may be based out of Tucson (Arizona, USA) or Indianapolis (Indiana, USA) with remote ...

LivaNova

Regulatory & Clinical Specialist

Phoenix, AZ · Remote

$85K - $95K/yr

Minimum of a master's degree in biomedical engineering, science or equivalent technical discipline ... This is a remote role (candidates must be based in the United States) * Occasional travel may be ...

Phoenix Staff

Lead Data & AI Engineer

Phoenix, AZ · On-site +1

$50 - $60/hr

Phoenix, AZ (hybrid remote) Type: 6-month contract to hire Pay: $50-60/hr We're looking for a Lead ... The position focuses on building modern data platforms, integrating diverse clinical and claims ...

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Remote Clinical Sas Programmer information

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How much do remote clinical sas programmer jobs pay per hour?

As of Sep 2, 2026, the average hourly pay for remote clinical sas programmer in Arizona is $50.36, according to ZipRecruiter salary data. Most workers in this role earn between $38.75 and $63.41 per hour, depending on experience, location, and employer.

What does a remote SAS clinical programmer do?

The job duties of a remote SAS clinical programmer involve programming within the Statistical Analysis System (SAS) software suite. You perform your responsibilities for this virtual job from a remote location outside of your client or employer’s office. A clinical SAS programmer focuses on clinical data collection and analysis. After gathering the required dataset, you analyze the data using SAS software to find the desired information about healthcare services, clinical trials, or other similar subjects. You then document the results of the analysis.

What is a remote clinical SAS programmer?

A Remote Clinical SAS Programmer is responsible for programming, validating, and analyzing clinical trial data using SAS software while working from a remote location. They collaborate with biostatisticians and clinical teams to create datasets, generate tables, listings, and figures, and ensure compliance with regulatory standards such as CDISC, SDTM, and ADaM. Their work supports drug development and regulatory submissions, making accuracy and efficiency crucial. Strong SAS programming skills, knowledge of clinical research, and experience with regulatory guidelines are essential for this role.

What does a remote clinical SAS programmer do?

As a Remote Clinical SAS Programmer, you'll primarily support clinical trial data analysis by programming tables, listings, and figures (TLFs), creating datasets, and ensuring data integrity. You will collaborate closely with biostatisticians, data managers, and other clinical team members to provide statistical outputs for clinical study reports and regulatory submissions. Your daily tasks include writing and validating SAS code, documenting work for audit purposes, and adhering to industry standards such as CDISC. The role often involves juggling multiple projects simultaneously, offering variety and opportunities to deepen your expertise in clinical data. This environment is well-suited to self-motivated professionals seeking both autonomy and collaborative teamwork in a dynamic, impactful field.

What are the key skills and qualifications needed to thrive as a remote clinical SAS programmer?

To thrive as a Remote Clinical SAS Programmer, you need strong statistical analysis skills, proficiency in SAS programming, and a background in clinical trials or life sciences. Experience with CDISC standards, clinical databases, and regulatory compliance, as well as certifications like SAS Certification or knowledge of SDTM and ADaM, are highly valued. Attention to detail, excellent communication, and time management are critical soft skills for remote collaboration and meeting project timelines. These attributes ensure reliable data outputs, successful teamwork, and compliance with industry regulations in a remote clinical research environment.

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Remote Clinical Sas Programmer jobs near you
Infographic showing various Remote Clinical Sas Programmer job openings in Arizona as of August 2026, with employment types broken down into 82% Full Time, 10% Part Time, and 8% Contract. Highlights an 100% Remote job distribution, with an average salary of $104,743 per year, or $50.4 per hour.

Biostatistician Expert - Remote

YO AI Labs

Phoenix, AZ • Remote

$60 - $70/hr

Full-time

Posted 22 days ago

Job description

Job Title: Biostatistician

Location: Remote
Job Type: Contractor
Pay: $60–$65/hour

Job Overview

We are looking for an experienced Biostatistician to support clinical research projects by analyzing clinical trial data, validating statistical outputs, and ensuring compliance with regulatory standards.

Key Responsibilities

  • Analyze and validate clinical trial data.

  • Review and interpret Statistical Analysis Plans (SAPs).

  • Produce and quality-check Tables, Figures & Listings (TFLs).

  • Review Clinical Study Reports (CSRs) and regulatory submission data.

  • Perform statistical analyses using SAS and/or R.

  • Collaborate with cross-functional teams and document findings accurately.

Required Skills

  • SAS and/or R

  • CDISC SDTM & ADaM

  • SAP interpretation

  • Survival analysis, mixed models, covariate adjustment

  • Multiplicity control & ICH E9(R1)

  • Clinical trial data analysis

  • TFL production & QC

  • Regulatory submissions & CSR review

  • Strong documentation, communication, and analytical skills

Qualifications

  • 5+ years of Biostatistics experience in clinical trials (Sponsor, CRO, or Academic Research).

  • MSc or PhD in Biostatistics, Statistics, or a related field.

  • Experience with regulatory submissions and statistical quality control is preferred.