Reference File Maintainer Nordic Countries
Madrid, Spain
hace 1 día

We are looking for a Reference File Maintainer Nordic Countries with experience to join our Multicultural team with more than 54 different nationalities.

The primary focus will be to be responsible for the maintenance of Product Reference Data of pharmaceutical and consumer health products in Sweden, Finland, Denmark and Norway.

The product data, which must be accurate, complete, and up to date, appears in a wide range of databases and publications used by the company's customers.

If you want to play a key role in a multicultural, dynamic and committed fun team this is a great opportunity.

Essential Functions

  • Update reference databases with new products and changes in the Nordic countries’ markets ensuring quality of the data : Classify products, standardize and group data following the company hierarchies and business rules
  • Investigate and analyze Swedish Consumer Health products.
  • Identify required changes to the existing reference file.
  • Work together with Local offices to identify when and how to correct inaccurate data, delete data, or add new entries to make the reference files more complete.
  • Produce files and outputs for specified production and quality control processes, client support activities, etc.
  • Identify and resolve routine exceptions and issues.
  • Perform quality control of maintained data and apply corrections as required.
  • Maintain documentation of processes and procedures.
  • Skills & other requirements :

  • High level of Swedish and mandatory High level English
  • Bachelor or Degree of Science preferably in Pharmacy or Life Science subject or work experience in pharmaceutical product information or in the pharmaceutical industry and / or have a familiarity with pharmaceutical and consumer health products and terminology.
  • Valuable experience maintaining and updating databases.
  • Computer literate.
  • Organizational skills. Good attention to detail with the ability to work accurately within tight deadlines.
  • Good team player
  • Ability to carry out moderate analysis and information gathering to resolve problems.
  • Experience of a production environment with workload prioritization would be advantageous

    We invite you to join IQVIA™

  • IQVIA recognized by Great Place to Work as the second best company to work for in Spain (March 2018)
  • FORTUNE Magazine's World's Most Admired Companies list for the third year in a row.
  • Recognised by the 2016 Scrip Awards as the Best Full-service Provider Contract Research Organization (CRO)
  • Awarded the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth consecutive year. A site-nominated award recognising contract research organizations (CRO) and biopharmaceutical sponsors dedicated to building positive relationships with research sites through leadership, professionalism and integrity.
  • IQVIA™ named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100® List which recognizes the world’s best service providers across a range of industries.
  • IQVIA™ is an equal opportunity employer . We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other "protected status.

    We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us .

    You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there!

    Reportar esta oferta

    Thank you for reporting this job!

    Your feedback will help us improve the quality of our services.

    Mi Correo Electrónico
    Al hacer clic en la opción "Continuar", doy mi consentimiento para que neuvoo procese mis datos de conformidad con lo establecido en su Política de privacidad . Puedo darme de baja o retirar mi autorización en cualquier momento.
    Formulario de postulación