1 to 4 of 4 Senior Statistical Programmer Jobs in the UK

Senior Statistical Programmer | Pharma | Fully Home Based | UK | Warman O’Brien are working with a Global Pharma who due to continued success and growth in the UK, have several opportunities for experienced Senior Statistical Programmers to join them. This is an exciting time to join … to work where you will get the chance to make your mark in doing good for others. What you will be doing: As a Senior Statistical Programmer, you will have an advanced knowledge of Statistical Programming and data structures and capabilities in leading Statistical Programming … technical and problem-solving skills to complete programming activities of high complexity and ambiguity that may benefit multiple project teams. Work either within Oncology Statistical Programming, Cell & Gene Therapy and Biopharma Statistical Programming or Exploratory Statistics. Use state-of-the-art methodology and the most innovative approach, generate more »

Our client is a global pharmaceutical brand who are expanding their programming and statistical teams. They are currently looking for senior level (and above) programmers who will be engaged on inital 12 month contracts on a fully remote basis. Programming is the department that oversees and delivers the more »

Statistical Programmer - multiple levels Home based #Oncology focused Our client, a global mid-size Pharma, have extended reputation in key therapeutic indications e.g. oncology, rheumatology, rare diseases, etc. and has supported the development of some of the most successful products. Through their particular focus on innovation and a more »

ICON people have a mission to succeed and a passion that ensures what we do, we do well. Responsibilities: Planning, managing and execution of statistical programming deliverables in clinical trial and non-trial activities in the project Providing input to authority required documents for the trial and non-trial … Ensuring that the inspection readiness documentation is updated at all time during the trial life cycle Required skills and experience: 5+ years' experience of statistical programming in clinical research or pharma Extensive experience with programming in e.g. SAS or R Experience of leading programming activities in clinical trial Experience … with reporting clinical trials, including statistical data handling, analysis and reporting Experience with review and documentation of programs Good knowledge of drug development Experience with clinical database technologies, data models and advanced programming Experience with collaboration across professional and regional borders Regular experience with communication and presentations In-depth more »