Ana Herradón Vírseda
TransCelerate Country Lead for Spain at TransCelerate BioPharma Inc.- Claim this Profile
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Bio
Experience
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TransCelerate BioPharma Inc.
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United States
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Pharmaceutical Manufacturing
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1 - 100 Employee
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TransCelerate Country Lead for Spain
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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
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TransCelerate Program Lead
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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.
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Bristol Myers Squibb
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United States
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Pharmaceutical Manufacturing
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700 & Above Employee
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Associate Director, Clinical Operations
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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.
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Sr. CDQM & Site Monitor Manager
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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.
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Interim Head of Clinical Operations
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Mar 2007 - Jun 2007
Interim Position
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Interim Site Monitor Manager - Germany, Austria & Switzerland
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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 .
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Clinical Site Manager
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Mar 2001 - Apr 2003
Project management activities for several Studies in different Therapeutic Areas.Main point of contact with the international team.
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C.R.A.
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Mar 2000 - Mar 2001
Clinical Research Associate responsibilities. Site selection, submision, recruitment, monitoring and closing activities.
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C.R.A.
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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
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Abbott
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United States
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Hospitals and Health Care
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700 & Above Employee
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Regulatory Assistant
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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.
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Abbott
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United States
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Hospitals and Health Care
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700 & Above Employee
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Regulatory Assistant
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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.
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Education
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Universidad Autónoma de Madrid
Master Degree, Biotechnology -
Universidad Politécnica de Madrid
Master Degree, Environmental Management -
Universidad Autónoma de Madrid
Bachelor Degree, Chemistry (Biochemistry and Molecular Biology)