JOIN ABBOTT AS A SENIOR DATA MANAGEMENT ANALYST IN WITNEY!

Are you passionate about data management and looking to make a significant impact? Abbott, a global healthcare leader, is seeking a Senior Data Management Analyst to join our team in Witney, UK.
At Abbott, we help people live more fully at all stages of life. Abbott is about the power of health. For more than 130 years, Abbott has been helping people reach their potential — because better health allows people and communities to achieve more. With a diverse, global network serving customers in more than 160 countries, we create new solutions — across the spectrum of health, around the world, for all stages of life. Whether it’s next-generation diagnostics, life-changing devices, science-based nutrition, or novel reformulations, we are advancing some of the most innovative and revolutionary technologies in healthcare, helping people live their best lives through better health.
Abbott Diabetes Care designs, develops, and manufactures leading-edge blood glucose monitoring technology for use in both home and hospital settings, including our revolutionary Freestyle Libre Flash Glucose Monitoring System.
As a result of strong business growth, industry-leading product development in the biosensor business, and a long-term commitment to manufacturing and innovation in our Witney Centre of Excellence, we have a fantastic opportunity for a Senior Data Management Analyst to join our expanding highly skilled team.

Your Role: As a Senior Data Management Analyst, you will:

• Lead and direct data management activities in support of R&D and clinical affairs.
• Develop data management processes, procedures, and best practices.
• Maintain effective data management systems to ensure all analysis and reporting requirements for project groups are met.
• Provide support and resources to the Statistics, Clinical Affairs, and Science Support Groups.
• Manage and support a multitude of interrelated software, data entry, verification, analysis, and reporting activities.
• Participate in clinical study teams and liaise with other departmental groups to establish priorities and communicate schedules.
• Support clinical studies, including CRF design/review, database build and validation, creation of data management documents, and laptop setups.
• Manage and contribute to the monitoring of tasks and metrics to ensure quality and provide reports on project/task status.
• Establish and support data systems and develop systems for tracking data and study progress.
• Review current practices and procedures to ensure compliance with regulatory policies and standards.
• Update and provide input into procedures, work instructions, and guidelines.

QUALIFICATIONS:

• Bachelor’s degree in a scientific or technical discipline or an equivalent combination of education and work experience.
• Minimum of 4 years of experience in data management.
• Proficiency in using word processor applications, spreadsheets, and databases.
  In addition to a competitive salary, Abbott offers a highly attractive benefits package which includes a defined-contribution pension scheme, a share ownership scheme, private healthcare, life assurance, and a flexible benefits scheme which you can tailor to your own requirements. Here at Witney, we also like to help our employees live life to the fullest, and therefore we offer a range of optional initiatives for you to get involved in, including couch to 5k campaigns, bee keeping, yoga, and more

• Lead and direct data management activities in support of R&D and clinical affairs.
• Develop data management processes, procedures, and best practices.
• Maintain effective data management systems to ensure all analysis and reporting requirements for project groups are met.
• Provide support and resources to the Statistics, Clinical Affairs, and Science Support Groups.
• Manage and support a multitude of interrelated software, data entry, verification, analysis, and reporting activities.
• Participate in clinical study teams and liaise with other departmental groups to establish priorities and communicate schedules.
• Support clinical studies, including CRF design/review, database build and validation, creation of data management documents, and laptop setups.
• Manage and contribute to the monitoring of tasks and metrics to ensure quality and provide reports on project/task status.
• Establish and support data systems and develop systems for tracking data and study progress.
• Review current practices and procedures to ensure compliance with regulatory policies and standards.
• Update and provide input into procedures, work instructions, and guidelines