Senior Statistical Programmer

🕒 June 5

🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

👻 Ghost score 16%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

Apply Now

Find Similar Remote Jobs

Set Up Email Alert For New Jobs

📊 Check your resume score for this job

Improve your chances of getting an interview by checking your resume score before you apply.

Upload Resume

Everest Clinical Research

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2004

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Everest Clinical Research is a global contract research organization (CRO) that provides end-to-end clinical trial services and biometrics expertise to pharmaceutical and biotechnology sponsors. The company offers clinical operations and project management, risk-based quality management and centralized monitoring, medical monitoring, pharmacovigilance, clinical data management, biostatistics and statistical programming, regulatory strategy and submissions, and technology solutions such as IRT/RTSM and ePRO/eCOA. Everest positions itself as a high-touch, quality-driven partner with global reach and therapeutic expertise across oncology, neurology, respiratory, rare diseases and immunology.

📋 Description

• Lead efforts in resolving day-to-day work-related issues and problems, ensuring quality of deliverables, as well as improving the efficiency and productivity of statistical programming work • Lead assigned projects by applying project management skills and statistical programming techniques; achieve on-time delivery of deliverables with quality, as well as earn client’s trust and repeat business • Develop SDTM and ADaM dataset specifications for CSRs, ISS, and ISE following company’s or client’s Standard Operating Procedures (SOPs) and project specific requirements • Perform quality control (QC) review of these documents prepared by others • Program and validate SDTM and ADaM datasets following approved dataset specifications for CSRs, ISS, and ISE • Perform CDISC standard compliant checks on SDTM and ADaM datasets • Generate, review, and resolve Pinnacle 21 validation issues • Perform additional QC checks on these deliverables using company Working Instruction (WI) QC checklists • Perform overall quality/consistency review of statistical TLGs before delivering them to the internal team or the client • Create SDTM and ADaM define.xml files • Perform QC review of these files prepared by others • Participate and/or lead programming teams in support of product regulatory submission related activities • Learn and maintain expertise in the use of the utilities and macros developed for the Statistical Programmers • Develop new macros and utilities • Program and perform QC/validation of complex data integrity checks to ensure data quality and ongoing scientific data surveillance • Complete job-required and project-specific training • Comply with applicable Everest and trial Sponsor’s Policies, SOPs, and WIs • Document data and programming information in accordance with corporate SOPs and guidelines • Archive clinical trial data (SDTM and ADaM datasets) and programming information in accordance with corporate archival SOPs and guidelines

🎯 Requirements

• A Master’s or Ph.D. degree in Statistics, Biostatistics, Epidemiology, and Computer Sciences, with at least four years’ experience in clinical trial statistical programming • A Bachelor’s degree in the above fields with at least six years’ experience in clinical trial statistical programming

🏖️ Benefits

• Flexible work arrangements • Professional development opportunities