
1001 - 5000 employees
Founded 1996
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą 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.
đ„ 3 minutes ago
đ§đ· Brazil â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ„ Software Engineer
đ» Ghost score 10%
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1001 - 5000 employees
Founded 1996
đ„ Healthcare
đŒ Consulting
đŠ Logistics
Healthcare âą Consulting âą 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.
âą Contribute to statistical programming activities related to global clinical trials âą Work closely with international teams of statisticians, programmers and data managers âą Program data sets and summaries âą Develop analysis data sets structure âą Develop program requirements and specifications âą Be involved in SAS programming of ADS and Tables, Listings and Figures âą Support SAS program validations âą Prepare and review program documentation âą Produce TFL âą Communicate with project teams and company departments regarding statistical programming of clinical research projects
âą University and Master's degree in applied science, mathematics, statistics or the like âą Knowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS system is desirable âą Good knowledge of programming logic, SQL and macro programming is preferred âą Proficient in English, spoken and written âą Experience within clinical trials and/or Biostatistics âą Good analytical skills âą Proficiency in standard MS Office applications âą Excellent communication and interpersonal skills âą CV must be submitted in English
âą Employees can work remotely âą Opportunity to work on global clinical trials and alongside international teams âą Exposure to medical science and development of new medicines
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