Website Everest Clinical Research
Your Quality and Data-Driven Global CRO
Location:Â Remote (Home-Based in Poland, near Warsaw preferred)
Company:Â Everest Clinical Research
Position:Â Senior Statistical Programmer
Also See: Data Center Design Architect
Join a Global Biometrics Center of Excellence in Poland
Everest Clinical Research is a premier global CRO renowned for high-quality deliverables, superior customer service, and entrepreneurial agility. We are entering an exciting growth phase with the establishment of a new Biometrics Center of Excellence in Poland. Over the next six months, we aim to build a dedicated team of 20+ biometrics experts. This is your opportunity to be a foundational member of a dynamic, remote-first team and help shape the future of clinical research from Poland.
The Role: Senior Statistical Programmer
We are seeking a highly skilled Senior Statistical Programmer to join our global biometrics team remotely from Poland. In this key role, you will lead programming efforts for clinical trial data, ensuring the highest quality and regulatory compliance for CSRs, ISS/ISE, and submissions. You will apply advanced SAS programming, CDISC standards (SDTM/ADaM), and project management skills to deliver critical datasets and outputs that drive drug development decisions.
Key Accountabilities:
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Manage and execute statistical programming deliverables for clinical studies, ensuring on-time, high-quality outputs that earn client trust and repeat business.
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Author and QC SDTM and ADaM dataset specifications. Program, validate, and deliver compliant datasets for regulatory submissions.
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Perform Pinnacle 21 validation and internal quality checks on datasets. Create and review define.xml files.
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Conduct overall quality and consistency reviews of statistical tables, listings, and figures (TLGs).
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Develop and maintain programming macros/utilities. Lead and mentor junior programmers, resolving day-to-day technical challenges to improve team efficiency.
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Program complex data integrity checks and ensure proper archival of clinical trial data and programming documentation per SOPs.
Required Qualifications:
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Option A: Master’s or PhD in Statistics, Biostatistics, Epidemiology, or Computer Science with 4+ years of clinical trial statistical programming experience.
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Option B: Bachelor’s degree in the above fields with 6+ years of clinical trial statistical programming experience.
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Expert proficiency in SAS programming for clinical trials within a pharmaceutical or CRO environment.
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Deep hands-on experience with CDISC standards:Â SDTM and ADaM implementation.
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Proven experience in the production and validation of datasets, TLGs, and supporting documentation for CSRs and regulatory submissions (ISS/ISE).
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Experience with Pinnacle 21 and other CDISC validation tools.
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Strong problem-solving skills, attention to detail, and a commitment to quality.
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Ability to work independently in a remote setting while collaborating effectively with global teams.
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Professional proficiency in English.
What We Offer:
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Contribute to global clinical trials and the development of new therapies.
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Be a pivotal member of a new, expanding Center of Excellence with clear advancement paths.
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Enjoy a permanent home-based role under our Work from Home policy.
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Join an established, growing CRO known for quality and customer focus.
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Attractive salary and comprehensive benefits package.
How to Apply:
If you are a dedicated statistical programming professional seeking a senior remote role with a growing industry leader, we encourage you to apply.
Submit your application via our official career portal:Â https://recruiting.ultipro.ca/EVE5000ECRC/JobBoard/0bec1c5f-4038-4ecd-a0fe-2e9d8620c772/OpportunityDetail?opportunityId=fbf86a72-7e40-4995-9b67-a3ee3405ea6d
Everest is committed to creating an inclusive environment and provides accommodations throughout the recruitment process. We thank all applicants, but only those selected for an interview will be contacted.