IQVIA Laboratories is looking for a Lead Programmer (Centralized Monitoring Analyst) in Rome, Italy. The role requires at least 3 years of relevant experience in pharmaceutical research and a minimum of 2-3 years of SAS programming experience. You
Product & Proposition Manager -Open Banking & Verification- Maternity Cover Full-time Employee Status: Regular Role Type: Hybrid Department: Product Management Schedule: Full Time Experian is a global data and technology company, powering opportunities for people and
Experian is a global data and technology company, powering opportunities for people and businesses around the world. We operate across a range of markets, from financial services to healthcare, automotive, agribusiness, insurance, and many more. Experian
This unique role within IQVIA lends itself to a Lead programmer on Cluepoints called Centralized Monitoring Analyst (CMA) with strong communication and organisation skills. Having experience with SAS programming is necessary. This role is part of a sponsor
Entra nel nostro mondo. Trasforma insieme a noi. Business Intelligence Analyst Quale sarà la tua sfida? Supporterai la delivery tecnica ed applicativa dei progetti in ambito Business Intelligence, svolgendo attività di analisi e sviluppo ed utilizzando
Role Overview You will offer end-to-end ownership of product development, from concept to go-to-market, working with diverse global teams across departments. It requires good understanding of client needs, building business cases, managing product roadmaps and scaling.
Premier Research is looking for a Statistical Scientist Director to join our Biostatistics team. You will help biotech, medtech, and specialty pharma companies transform life‑changing ideas and breakthrough science into new medicines, devices, and diagnostics. What
Syneos Health is seeking a Principal Statistical Programmer (European Timezone Only) for a 1.5-year temporary assignment. You will lead programming activities, develop SAS-based analyses, and mentor junior programmers, collaborating with statisticians and stakeholders across trials in Europe. Eligible