🔥 11 hours ago
Lead SAS statistical programmer developing and validating clinical-trial outputs for Syneos Health, a global life sciences services organization. Guiding programming teams and supporting drug development projects.
🕒 3 days ago
Principal Statistical Programmer developing SAS/R datasets, tables, graphs, and regulatory deliverables for Cytel’s pharmaceutical clients. Overseeing CRO programming and supporting clinical development studies across therapeutic areas.
Java
Linux
Python
Unix
🕒 3 days ago
Principal Statistical Programmer developing SAS/R datasets, tables, graphs, and regulatory outputs for Cytel’s pharmaceutical clinical-trial programs. Overseeing CRO deliverables and supporting submissions across multiple studies.
Java
Linux
Python
Unix
🕒 5 days ago
Statistical Programmer developing SAS-based SDTM, ADaM, and TFL outputs for Fortrea’s global pharmaceutical clients. Supporting complex phase I–III clinical-trial programming, quality control, and regulatory submissions.
🕒 August 3
Statistical Programmer II at Syneos Health working collaboratively across drug development. Engage with innovative teams to deliver valuable insights and solutions in clinical trials.
🕒 August 3
Sr Statistical Programmer developing statistical tables and listings using SAS at Syneos Health. Collaborating with teams to ensure project deliverables meet quality standards and regulatory guidelines.
🕒 July 31
Statistical Programmer developing custom programming code in SAS for clinical data analysis. Collaborating with clinical teams to ensure quality outputs and timely delivery of project specifications.
🕒 July 30
Manager of Statistical Programming creating SAS programs for data analysis at Bristol Myers Squibb. Collaborating with project teams and ensuring quality deliverables in the field of biostatistics.
🏖️ New Jersey – Remote
💵 $158.3k - $179.3k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
🕒 July 29
Responsible for applying biostatistical methods supporting clinical trials and data management at Alimentiv. Involves statistical analysis, project collaboration, and regulatory reporting.
🕒 July 28
Principal Statistical Programmer Consultant working for ClinChoice supporting a global CRO. Engaging in clinical trial data analysis and project collaboration with clients.
🕒 July 28
Principal Statistical Programmer focused on clinical development for a global pharmaceutical client. Working independently and overseeing CRO programmers while ensuring high-quality data summaries.
🕒 July 28
Senior Statistical Programmer at Cytel, leveraging SAS programming for global clinical trials in pharmaceuticals. Collaborating with cross-functional teams to ensure quality data analysis and reporting.
🕒 July 28
Principal Statistical Programmer at Syneos Health developing statistical programs using SAS. Collaborating with stakeholders and mentoring junior programmers in a clinical setting.
🕒 July 27
Senior Statistical Programmer developing SAS programs for clinical trial datasets and outputs. Collaborating with teams and mentoring junior programmers with a focus on compliance and quality control.
🌲 North Carolina – Remote
💵 $104.8k - $128k / year
💰 Private Equity Round - WCG on 2019-11
⏰ Full Time
🟠 Senior
🖥 Software Engineer
🕒 July 27
Senior Principal Statistical Programmer leading statistical programming efforts for clinical trials. Collaborating with biostatistics, project management and data management teams for high-quality statistical outputs.
🌲 North Carolina – Remote
💵 $131.1k - $160k / year
💰 Private Equity Round - WCG on 2019-11
⏰ Full Time
🟠 Senior
🖥 Software Engineer
🕒 July 27
Senior Statistical Programmer at Edetek focusing on statistical programming for pharmaceutical projects. Collaborating with biostatisticians and mentoring junior staff in data analysis and compliance standards.
🕒 July 27
Senior Statistical Programmer leveraging advanced SAS programming skills to support clinical trials. Working fully embedded with pharmaceutical clients and contributing to patient treatment outcomes.
🕒 July 24
Contract Statistical Programmer at Iovance Biotherapeutics developing and maintaining programming deliverables in cancer treatment. Collaborating with cross-functional teams to deliver timely datasets for clinical studies.
🇺🇸 United States – Remote
💵 $70k - $80k / year
⏳ Contract/Temporary
🟡 Mid-level
🟠 Senior
🖥 Software Engineer
🕒 July 24
Contract Statistical Programmer at Iovance Biotherapeutics developing and maintaining programming deliverables in cancer treatment. Collaborating with cross-functional teams to deliver timely datasets for clinical studies.
🇺🇸 United States – Remote
💵 $70k - $80k / year
⏳ Contract/Temporary
🟡 Mid-level
🟠 Senior
🖥 Software Engineer
+57 More Statistical Programmer Jobs Available!

The average salary for remote statistical programmers is $155,819 per year. This is based on data from 346 job openings. Our advanced AI searches the internet for remote job openings and posts them on our website. We use the salary data from these job postings to calculate salary expectations.
Below is a breakdown of salary data by years of experience:
| Experience | Number of roles analyzed | Average Salary |
|---|---|---|
⚪️ Entry-level Statistical Programmer (0 yrs) | 1 | $0 |
🟢 Junior Statistical Programmer (1-2 yrs) | 12 | $106,474 |
🟡 Mid-level Statistical Programmer (2-4 yrs) | 43 | $140,813 |
🟠 Senior Statistical Programmer (5-9 yrs) | 203 | $159,392 |
🔴 Lead Statistical Programmer (10+ yrs) | 87 | $163,494 |
We analyzed 266 job listings in the last year and found it takes about 49 days for employers to close a job opening.
We reviewed 346 job postings and found the top 10 skills employers are asking for most often are:
You need strong statistical analysis skills, proficiency in programming languages such as SAS, R, or Python, and a solid understanding of statistical methodologies. Attention to detail, problem-solving abilities, and good communication skills are also important for remote work.
Typically, a degree in statistics, mathematics, computer science, or a related field is required. Additional certifications in statistical programming or data analysis can be advantageous. Experience with data management and analysis is often emphasized.
Responsibilities include designing and validating statistical programs, analyzing clinical trial data, generating reports, and ensuring compliance with regulatory standards. You'll also collaborate with cross-functional teams and communicate findings effectively.
Benefits include flexible working hours, the ability to work from any location, reduced commuting time, a better work-life balance, and exposure to diverse projects and teams globally.
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We find jobs as soon as they're posted, so you can apply before everyone else.
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