Ana Herradón Vírseda

TransCelerate Country Lead for Spain at TransCelerate BioPharma Inc.
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Contact Information
us****@****om
(386) 825-5501
Location
Greater Madrid Metropolitan Area, ES

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Experience

    • United States
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • TransCelerate Country Lead for Spain
      • Jan 2018 - Present

      Bring knowledge of the TransCelerate portfolio and assets to Member Company resources within SpainEnhance voluntary global adoption Raise awareness about TransCelerate globally amongst key stakeholders

    • TransCelerate Program Lead
      • Sep 2016 - Jun 2020

      TransCelerate Program Lead for BMS, responsible of the internal TransCelerate awareness, creating an internal network to support and maximize solutions adoptions.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Associate Director, Clinical Operations
      • Jun 2017 - Present

      Responsible for a team of Clinical Site Monitors and Clinical Site Data Monitoring, part of the Iberia Clinical Operations Organization, to ensure the execution of the Iberian book of work in terms of recruitment, monitoring and data quality.

    • Sr. CDQM & Site Monitor Manager
      • May 2003 - Present

      Responsible for a team of Clinical Site Monitors & Clinical Data Quality Managers, part of the Iberia Clinical Operations Organization Main tasks are resource management, staff selection, development, & performance. Ensure the execution of the Iberian book of work in terms of recruitment, monitoring & data quality.

    • Interim Head of Clinical Operations
      • Mar 2007 - Jun 2007

      Interim Position

    • Interim Site Monitor Manager - Germany, Austria & Switzerland
      • Sep 2005 - Mar 2006

      Interim PosotionResponsible for a team of Clinical Site Monitors,part of the Germany, Austria and Switzerland Clinical Operations Organization Main tasks are resource management, staff selection, development, & performance. Ensure the execution of the book of work in terms of recruitment and site monitoring .

    • Clinical Site Manager
      • Mar 2001 - Apr 2003

      Project management activities for several Studies in different Therapeutic Areas.Main point of contact with the international team.

    • C.R.A.
      • Mar 2000 - Mar 2001

      Clinical Research Associate responsibilities. Site selection, submision, recruitment, monitoring and closing activities.

    • C.R.A.
      • Sep 1998 - Mar 2000

      As contractor for Abbott Laboratories, S.A. Clinical Research Associate responsibilities. Site selection, submision, recruitment, monitoring and closing activities As contractor for Abbott Laboratories, S.A. Clinical Research Associate responsibilities. Site selection, submision, recruitment, monitoring and closing activities

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Regulatory Assistant
      • Feb 1998 - Sep 1998

      As Freelance Review and development of local packaging and inserts for nutricionals products & medical devices to ensure compliance with local regulation. As Freelance Review and development of local packaging and inserts for nutricionals products & medical devices to ensure compliance with local regulation.

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Regulatory Assistant
      • Apr 1996 - Sep 1997

      Review and development of local packaging and inserts for nutricionals products & medical devices to ensure compliance with local regulation. Review and development of local packaging and inserts for nutricionals products & medical devices to ensure compliance with local regulation.

Education

  • Universidad Autónoma de Madrid
    Master Degree, Biotechnology
    1998 - 1999
  • Universidad Politécnica de Madrid
    Master Degree, Environmental Management
    1997 - 1998
  • Universidad Autónoma de Madrid
    Bachelor Degree, Chemistry (Biochemistry and Molecular Biology)
    1990 - 1996

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