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Abbott; United Kingdom

     Published: April 30, 2024   08:12

     
                        
Duties: We currently have opportunities for a Statistician to join our team! This could be based from our Medical Devices Centre of Excellence in Witney, Oxfordshire, or from our Maidenhead office
Requirements: We are therefore keen to hear from candidates qualified to Degree level in Mathematics, Statistics or similar, who are looking for an opportunity to make an impact at work and contribute to patient health for the next generation of glucose-monitoring technology. You will need to have good oral and written communication skills to be able to collaborate with different people within the department, prepare reports, interpret results, and provide effective summaries for specialist and non-specialist audiences. You must be organised and flexible in your approach to work, with good attention to detail in order to ensure that data and analyses are accurate. Industry based experience is required, and programming skills in SAS would be advantageous

Abbott; Alameda, California, United States

     Published: April 28, 2024   10:50

     
                        
Duties: Project Management toolkit; Ensure that database design is consistent with 21 CFR part 11; Provide input to the development of case report forms, in conjunction with Clinical Research and Clinical Data Specialists; Annotate CRFs and develop study clinical databases using Oracle Clinical or other clinical database; In conjunction with Clinical Data Specialists, write study specific data entry work instructions; In conjunction with the Validation team, ensure databases are validated and data entry training has been provided before the database is activated; With Clinical Research staff and Clinical Data Specialists, contribute to the development of data edit check rules
Requirements: Bachelors’ degree required. Management, Psychology, Information science, public health, or life science preferred; Minimum of 3 years’ experience in clinical research and database programming; prefer at least 1 year in device or pharmaceutical clinical trials as a clinical programmer performing mentioned above functions using SAS, Oracle Clinical or Clintrial and/or ACCESS

Abbott; United Kingdom

     Published: April 28, 2024   10:50

     
                        
Duties: Transfer of products and processes from Research & Development into Manufacturing to support our exciting new product launches; Investigation and monitoring of manufacturing, stability and product performance data to drive continuous improvement; To be a key individual for development trials and analytical test methods utilising your statistical background (e.g. Design of Experiments, Analysis of Variance, setting acceptance criteria & capability analysis) to drive quality and business decisions; Utilising your passion for team leadership, people management, and talent development/mentoring
Requirements: You will have a BSc (or higher) in Statistics or Mathematics. Previous experience working in a regulated or manufacturing environment, and SAS/R programming are advantageous

Abbott; United Kingdom

     Published: April 28, 2024   10:50

     
                        
Duties: We currently have an exciting opportunity for a Senior Statistician to join our Technical Operations Statistics team to provide statistical expertise across the ADC product range collaborating with Technical, Manufacturing, Research & Development, Engineering, Quality and Regulatory colleagues
Requirements: You will have a BSc (or higher) in Statistics or Mathematics. Previous experience working in a regulated or manufacturing environment, and SAS/R programming are advantageous

Abbott; Weesp, Netherlands

     Published: April 17, 2024   08:03

     
                        
Duties: Coordinates, provides and delivers methodological and statistical expertise and/or statistical analyses for clinical studies in EPD. In this matter supports both the Clinical Development portfolio as well as Strategic Medical Affairs in their support to Affiliates, thereby complying with international, regulatory guidelines and EPD policies and standards. Directs the operational aspects of statistical work as outsourced to CROs
Requirements: MSc./PhD in Statistics, or Biostatistics, or a related field; Demonstrated high competence in experimental design and statistical inference. Thorough understanding of International Conference on Harmonization (ICH) Guideline and relevant regulatory requirements (e.g., EU, US, or China). Minimum 7 years experience as Statistician in pharmaceutical industry or CRO

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