Selected: ✨ Statistical Programmer.
Selected: 🆕 Date Added.
🔥 22 hours ago
Statistical Programmer II producing SAS-based clinical trial datasets, tables, figures, and reports for Parexel’s clinical research programs. Supporting compliant statistical programming for global sponsors.
🌐 Poland, Romania, +2 more countries – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟡 Mid-level
🟠 Senior
🖥 Software Engineer
👻 Ghost score 10%
🕒 Yesterday
Principal Statistical Programmer developing and validating R programs, SDTM, and ADaM outputs for ICON’s sponsor-dedicated clinical research teams. Supporting regulatory-quality analyses and statistical reporting.
🕒 Yesterday
Lead SAS statistical programming for Syneos Health’s clinical drug-development services. Manage clinical trial outputs, validation, documentation, and programming teams.
🕒 Yesterday
Lead statistical programming for Syneos Health’s clinical drug development services. Developing SAS outputs, validating CDISC deliverables, and guiding programming teams.
🕒 Yesterday
Senior Statistical Programmer leading CDISC-compliant SAS and R programming for Cencora’s pharmaceutical and biotechnology research operations. Coordinating regulatory submissions, datasets, TFLs, and documentation across teams.
🕒 2 days ago
Principal Statistical Programmer leading SAS/CDISC programming for Syneos Health’s clinical-trial and regulatory submissions. Developing validated datasets, outputs, and standards across complex global projects.
🕒 6 days ago
Principal Statistical Programmer supporting oncology clinical trials at Cytel, a provider of statistical software and clinical-trial analytics. Developing SAS outputs, CDISC datasets and regulatory submission materials.
🌐 United Kingdom, South Africa, +1 more countries – Remote
⏰ Full Time
🔴 Lead
🖥 Software Engineer
👻 Ghost score 21%
Java
Linux
Python
Unix
🕒 September 16
Senior Statistical Programmer using SAS and CDISC standards for a pharmaceutical client. Supporting clinical-trial data analysis, submissions, validation, and global study teams.
🕒 September 16
Senior SAS Programmer supporting Parexel’s clinical trials through statistical programming, data analysis, and regulatory reporting. Leading global teams and ensuring quality, timelines, budgets, and compliance.
🌐 United Kingdom, Hungary, +2 more countries – Remote
💰 Venture Round on 1990-01
⏰ Full Time
🟠 Senior
🖥 Software Engineer
🇬🇧 UK Skilled Worker Visa Sponsor
👻 Ghost score 10%
Google Cloud Platform
🕒 September 15
Biostatistician developing statistical analysis plans, SAS analyses, and reports for Celerion’s clinical research programs. Supporting randomization, data interpretation, and client deliverables.
🕒 September 15
Biostatistician developing analysis plans and conducting SAS analyses for Celerion’s clinical research programs. Preparing statistical reports and supporting clinical study randomization.
🇺🇸 United States – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
👻 Ghost score 10%
🕒 September 15
Senior Statistical Programmer leading SDTM, ADaM, and TLF programming for Indero, a dermatology contract research organization. Delivering validated clinical-trial data and regulatory submission packages remotely in the Philippines.
🕒 September 15
Senior Statistical Programmer leading SAS and CDISC programming for Indero, a dermatology-focused CRO. Delivering validated clinical-trial datasets, TLFs, and regulatory submission packages remotely from India.
🕒 September 15
Senior Statistical Programmer leading SAS and CDISC programming for clinical trials at Indero, a dermatology-focused CRO. Developing validated SDTM, ADaM, TLF, and regulatory submission deliverables.
🕒 September 15
Biostatistician leading statistical activities for Indero, a dermatology-focused contract research organization. Supporting Phase 1–4 trials, SAPs, CDISC analyses, budgets, and clinical study reports.
🕒 September 14
Lead statistical programming for Syneos Health’s China-dedicated clinical trial services. Developing and validating SAS outputs, guiding programmers, and supporting sponsor-facing study activities.
🕒 September 8
Senior Statistical Programmer supporting CDISC clinical study programming for ClinChoice, a global full-service CRO. Delivering compliant analyses, specifications, documentation, and quality-focused programming.
🕒 September 7
Lead statistical programming for Syneos Health’s clinical drug development services. Developing and validating SAS outputs, managing deliverables, and mentoring programming teams.
🕒 September 2
Senior Statistical Programmer developing SAS datasets and statistical reports for Everest, a full-service clinical research organization. Validating clinical trial analyses and guiding statistical programming standards.
🏖️ New Jersey – Remote
💵 $90k - $140k / year
⏰ Full Time
🟠 Senior
🖥 Software Engineer
🦅 H1B Visa Sponsor
👻 Ghost score 0%
🕒 September 2
Principal Statistical Programmer developing SAS clinical-trial outputs for Syneos Health’s integrated life-sciences services. Leading statistical programming, CDISC compliance, submissions, and programmer mentoring.
+60 More Statistical Programmer Jobs Available!

The average salary for remote statistical programmers is $152,011 per year. This is based on data from 380 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) | 15 | $103,754 |
🟡 Mid-level Statistical Programmer (2-4 yrs) | 49 | $140,813 |
🟠 Senior Statistical Programmer (5-9 yrs) | 223 | $156,578 |
🔴 Lead Statistical Programmer (10+ yrs) | 92 | $156,425 |
We analyzed 292 job listings in the last year and found it takes about 50 days for employers to close a job opening.
We reviewed 380 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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