9 Statistical Programmer Jobs

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 this inspiring … 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 activities and … 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 »

Clinical Statistical Programmer; Global Pharma, Oncology - Remote - Permanent Proclinical is seeking a dedicated Clinical Statistical Programmer with a focus on Oncology. This is a remote permanent position. Primary Responsibilities: In this role, you will apply your biostatistics skills and experience to support the development of scientifically … part of our Global Biostatistics department, collaborating with multiple functional areas across the company. Skills & Requirements: Advanced degree (MSc or PhD). Proficiency in statistical programming, particularly SAS. Detailed knowledge of CDISC standards (SDTM, ADAM). Excellent communication skills, both written and verbal, with the ability to communicate complex … statistical concepts to non-statistical audiences. Ability to work effectively in a team environment and to manage multiple projects simultaneously. Attention to detail and the ability to prioritize tasks and meet tight timelines. The Clinical Statistical Programmer will: Support analysis and reporting on clinical projects. Collaborate more »

Proclinical are seeking a dedicated Senior Statistical Programmer to join a dynamic team committed to advancing and improving patients' lives. This position is a permanent opportunity and is remote based role anywhere within the UK. Responsibilities: * Lead and manage programming deliverables on multiple projects, ensuring quality and timely … and workload tracking in line with agreed metrics. * Develop and foster client relationships through effective project management and communication. Requirements: * Extensive experience as a Statistical Programmer, preferably in the clinical research industry. * Bachelor's degree in a quantitative or scientific discipline. * Proficiency in SAS, with the ability to 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 »

Pharma are partnered with a global Pharmaceutical company who are sitting in the top 10 pharmaceutical companies in the world. We have a few statistical programmer roles within this company at varying seniority levels. The Candidate : Must have experience with SAS and R For higher level someone with more »

NJ, USA and presence in other 20+ countries-India, Denmark, UK, Singapore etc. (www.tech-observer.com) We are hiring for following roles on FSP: a. Statistical programmers : 5-8 years of exp in clinical SAS Programming Senior Statistical Programmers : 8-12 years of exp in clinical SAS Programming b. … Principal Statistical programmers : 12+ years of exp in clinical SAS Programming Location -United Kingdom (candidates eligible to work in UK shall be considered) Work Timings : US Timings (EST -3 days and PST -2 days) Job Responsibilities- 1.Compliance with working SOPs within the framework of the Quality Management System and … guidelines. 2. Implement and follow the latest versions of CDISC, FDA Guidelines, GCP and other industry standards. 3. Participate in and co-ordinate the Statistical Programming review of Case Report Forms (CRFs), annotated CRFs, database structures and study related documentation (e.g. data validation guidelines). 4. Review and interpret 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 programming 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 »

programming activities with minimal supervision. Able to identify gaps in current programming best practices and offer suggestions for improvement. Minimum 3 year experience within Statistical Programming in a clinical environment. What ICON can offer you: Our success depends on the quality of our people. That’s why we’ve more »