Senior Data Analyst

England, North Yorkshire, York
£27000.00 - £30000.00 per annum
10 Sep 2020
08 Oct 2020
JN -092020-141011
Amanda Allcock
Contract Type
Full Time

This person will be responsible for the following operational areas,

  • Manage and enhance utilisation of SAS commercial application for management of client data.
  • Assume responsibility for data management and functionality and deliverables on the program level for their clients
  • Assume responsibility for regional and global clinical studies from database set up through database lock, including the creation of Data Management Agreement, data cleaning plan, definition and validation of edit checks, data review and coding and data reconciliation.
  • Generate cumulative or incremental data files for protocols and provide QC'd data-sets in accordance with client specifications.
  • Maintain internal client tracking documentation to allow the collection of metrics and key performance indicators.
  • Communicate and participate in teleconference with sponsors and CROs about data file transmission schedules and formats.
  • Support Client and internal Audits and regulatory inspections in collaboration with Director of Study Management and US Manager of Data Management.
  • Coordinate data transfers and data harmonisation for clinical trials and communicate data management specifications with all assigned clients.
  • Perform and develop reporting requirements for both internal and external clients from the clinical database as needed.
  • Support other data analysts in their duties and provide cover for holidays and sickness
  • Develop and implement improvements to existing data management programs and reports to improve functionality and/or efficiency
  • Provide support to the Clinaxys Database Administrator(s) as required to cover planned and unplanned absence or periods of high demand.

The post-holder is responsible for ensuring that all the above processes are performed in accordance with:

  • Definitive study protocols
  • The current ICH Guideline for Good Clinical Practice
  • UK Clinical Trial Statutory Instruments
  • Current Health and Safety Legislation and Human Resources policies.
  • Other legislation that is relevant to the responsibilities of the post
  • Standard operating procedures

Qualification Requirements

BSc in a relevant discipline and/or at least 2 years relevant experience

Adecco acts as an employment agency for permanent recruitment and an employment business for the supply of temporary workers. The Adecco Group UK & Ireland is an Equal Opportunities Employer.

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