TMF Quality Project Lead
IQVIA
Buenos Aires, AR
hace 2 días
source : DirectEmployers Association

This is an exciting opportunity for TMF Quality Project Lead role within Records Management department. If you are motivated, experienced in cross functional collaboration, have strong communication skills and consider yourself as a good team leader, please review and apply! Job Overview Serve as the liaison between Records Management and user departments regarding Trial Master files.

Apply Records Management expertise to provide project related assistance. Ensure all work is conducted in accordance with Standard Operating Procedures (SOPs), policies, practices, good clinical practices, applicable regulatory requirements, and meets quality and timeline metrics.

Essential Functions + Ensure project deadlines, commitments, and goals are met by monitoring team's daily outputs.+ Coordinate the retrieval of records requested by users and prepare closed studies for transfer to clients.

  • Monitor filing accuracy and compliance to IQVIA or customer file plans and Standard Operating Procedures (SOPs).+ Maintain records center security to protect record integrity by ensuring compliance to SOPs.
  • Interface with departments to support retrieval projects and ensure information needs are met.+ Monitor and assist in the preparation of closed studies for transfer to clients per agreed due dates.
  • Serve as primary contact for clients.+ Collect data and assist in the preparation of statistical reports for management of record center operations, as appropriate or as requested.
  • Coordinate transfer, recall, and disposition of records to commercial records storage centers.+ Assist management with the implementation of strategic goals, plans, cost proposals, and resource projections for records management projects.
  • May function as team leader for records management projects. Qualifications + Bachelor s Degree in Life Sciences or related field.
  • At least 3 years' experience working in a Records Management environment.+ Strong oral and written communication skills and good command of English Language.
  • Strong knowledge of applicable research and regulatory requirements, , International Conference on Harmonization (ICH), Good Clinical Practice (GCP) and relevant local laws, regulations and guidelines.
  • Knowledge of technology applications relevant to records management environments.+ Ability to handle multiple tasks and projects within defined timelines and balance competing priorities.
  • Ability to establish and maintain effective working relationships with internal and external clients.At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible - to help our customers create a healthier world.
  • The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.

    Learn more at IQVIA is a world leader in using data, technology, advanced analytics, and expertise to help customers drive healthcare - and human health - forward.

    Together with the companies we serve, we are enabling a more modern, more effective and more efficient healthcare system, and creating breakthrough solutions that transform business and patient outcomes.

    To get there, it takes diverse skills and a curiosity to explore new possibilities. No matter your role, everyone at IQVIA, including our colleagues at Q² Solutions, contributes to our shared goal of improving human health.

    Thank you for your interest in growing your career with us.EEO Minorities / Females / Protected Veterans / Disabled

    Reportar esta oferta
    checkmark

    Thank you for reporting this job!

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

    Inscribirse
    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.
    Continuar
    Formulario de postulación