1 to 10 of 10 Statistical Programmer Jobs

and more efficient ways to design, capture, manage, review, and visualize clinical trial data. We are currently looking for an enthusiastic and talented Senior Statistical Programmer willing to be involved in all spectrum of Statistical Programming activities, including acting as Lead Programmer on studies. This role … the UK or EU where we have the ability to hire. Your core responsibilities: Creation and QC of study specifications for SDTM datasets, and statistical programming and QC of SDTM datasets for Phase I-IV trials. Creation and QC of study specifications for ADaM datasets, and statistical programming … and QC of ADaM datasets for Phase I-IV trials. Statistical programming and QC of tables, listings and figures for Phase I-IV trials. Responsible for the quality and timeliness of assigned statistical deliverables. As Lead Statistical Programmer, primarily responsible for all statistical programming activities more »

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 »

Principal Statistical Programmer | Leading CRO | UK | Home Based Award winning global CRO have a new opportunity for a Principal Statistical Programmer to join their dynamic and expanding team. This is a fully home-based position based in the UK. This is a Statistical Programming leadership … do next: If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the new Principal Statistical Programmer onboard as soon as possible. Not what you’re looking for? Please contact Jo Fornaciari on 0330 335 9476 for a confidential more »

Because humanity needs solutions, fast. Data Sciences at Quotient comprises over 100 staff and provides an expert service in the data management, pharmacokinetics, programming, statistical analysis and reporting of early Phase clinical studies. Due to our continued growth and success we have an excellent career opportunity for a talented … Programmer to join our Statistical Programming department and further your career. You will be involved in the challenging environment of early phase clinical studies and play a key role in the expansion and continuous development of our statistical programming services. Main tasks and responsibilities include: Generate SDTM … time, and progress to more senior roles and tasks. Training will be provided to help your further your programming skills and achieve a Lead Statistical Programmer role within Data Sciences project teams. Experienced candidates may also become involved in staff training/mentoring, sponsor contact and where relevant 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 »

Proclinical is seeking a dedicated Principal Statistical Programmer to become part of a global Biostatistics and Programming team. This role is an instrumental part in running and overseeing programming at the study and program level as well as ensuring all work is of the highest quality standards. Responsibilities 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 »

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 »