Live opening · Posted 7 hours ago

Mid-Senior Statistical Programmers- Remote (Europe / EU)

NoyMed CRO · Poland (Remote)
Linkedin Yes
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At a glance

The key details from the original listing.

Posted 7 hours ago
CompanyNoyMed CRO
LocationPoland (Remote)
Work modeYes
SkillsGCP
SourceLinkedin
ListedPosted 7 hours ago

About the role

Description supplied by the original job listing.

NoyMed CRO is hiring Mid-Senior Statistical Programmers to join our team. In these roles, you will deliver statistical programming solutions for clinical trials. We are looking for programmers with clear communication skills and practical problem-solving abilities to contribute to our clinical research projects.
Key Responsibilities
Conduct work consistent with GCP, ICH, 21 CFR Part 11, internal SOPs, and international regulatory requirements.
Develop and validate specifications, algorithms, and programs for SDTM and ADaM datasets following CDISC implementation guides and Statistical Analysis Plans (SAP).
Create, upgrade, and validate programs to produce Tables, Listings, and Graphs (TLGs), maintaining data accuracy, traceability, and reproducibility.
Build SAS macros to automate and standardize routine data workflows.
Lead statistical programming activities, oversee project plans, track daily status and timelines, monitor budgets, and communicate directly with clients and project statisticians (when assigned).
Serve as mentors and guides for junior programmers.
Qualifications
Bachelor’s degree in Computer Science, Mathematics, Statistics, or a related field.
3+ years of relevant work experience in statistical programming for clinical research.
SAS programming language experience is required (SAS Certification preferred).
Proficiency in R, SQL, or other programming tools is preferred.
Prior experience in a leading role, managing project timelines, or mentoring team members is a plus.
Professional English skills, both written and spoken; knowledge of additional languages is a plus.
Applied knowledge of data collection, data flow, extraction, and CDISC standards (SDTM, ADaM).
Practical understanding of research processes, clinical operations, and data quality management.
Attention to detail and the ability to manage multiple tasks, prioritize workload, and work independently.
This role is 100% remote and open to applicants located anywhere in the European Union / Europe.
If you are interested in this position, please apply now via LinkedIn or by sending your CV to career@noymed.com, mentioning “SAS Programmer” in the Subject Line of your e-mail.
Please note that only shortlisted candidates will be contacted for the interview.

Work arrangement
Yes

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