SAS Programmer I

Job not on LinkedIn

🕒 February 20

🇧🇷 Brazil – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🖥 Software Engineer

👻 Ghost score 45%

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.

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PSI CRO AG

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

Founded 1996

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

PSI CRO AG is a global contract research organization (CRO) that specializes in conducting clinical trials. The company focuses on delivering pivotal Phase 2 and 3 clinical trials across various therapeutic areas, including Inflammatory Bowel Diseases, Oncology, Hematology, Infectious Diseases, Multiple Sclerosis, and Rare Diseases. PSI utilizes a proprietary technology platform for clinical trial planning and financial tracking to ensure trials are conducted on time and within budget. The company is recognized for its expertise, quality, compatibility, and reliability, having been awarded the CRO Leadership Awards for multiple consecutive years.

📋 Description

• Develop analysis data sets structure • Develop program requirements and specifications • Be involved in SAS programming of ADS and Tables, Listings and Figures • Support SAS program validations • Prepare and review program documentation • Produce TFL • Communicate with project teams and company departments with regard to statistical programming of clinical research projects

🎯 Requirements

• University and Master's degree in applied science, mathematics, statistics or the like • Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system is desirable • Good knowledge of programming logic, SQL and macro programming is preferred • Proficient in English, spoken and written • Experience within clinical trials and/or Biostatistics • Good analytical skills • Proficiency in standard MS Office applications • Excellent communication and interpersonal skills

🏖️ Benefits

• Flexible work arrangements • Professional development • Health insurance