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IQVIA
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Milan,
Italy
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scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International ... ongoing project expectations and issues.
• Evaluate the quality and integrity of study site practices
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IQVIA
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Milan,
Italy
...
regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization ... issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of
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IQVIA
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Frankfurt,
Germany
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Join IQVIA as a CRA / SrCRA (m/w//d) in our Clinical Site Management department home-based throughout Germany. You will focus on a comprehensive clinical trial management in a variety of indications
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IQVIA
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New Cairo,
Egypt
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Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with ... issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of
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IQVIA
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Athens,
Greece
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Clinical Practice.
• Work with sites to adapt, drive, and track subject recruitment plan in line with ... issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of
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IQVIA
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Paris,
France
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IQVIA Clinical Functional Services Partnerships (FSP) business is unique. Our teams are dedicated to a single sponsor partner, where the common goal is quality delivery for our customers. We set
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IQVIA
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Milan,
Italy
...
regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization ... issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of
...
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IQVIA
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Stevenage,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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Chesterfield,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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Leeds,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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Brighton,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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Reading,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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Livingston,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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Cambridge,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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Bath,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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London,
United Kingdom
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Clinical Research Associate (all levels) Sponsor Dedicated, Home Based, UK
**Join us on ... Dedicated (cFSP) team are growing, join us on our mission to drive healthcare forward!
As Clinical
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IQVIA
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Reading,
United Kingdom
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IQVIA UK are seeking Clinical Research Associates (CRA II / SR CRA) to strengthen our cFSP (sponsor ... ., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work
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IQVIA
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Netanya,
Israel
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regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization ... issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of
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IQVIA
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Oslo,
Norway
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regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization ... issues.
• Evaluate the quality and integrity of study site practices related to the proper conduct of
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IQVIA
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London,
United Kingdom
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making the CRA role more efficient and discussions at site more productive. Next generation clinical ... contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International
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IQVIA
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Poland
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productive. Next generation clinical development!
We offer genuine career development opportunities for ... requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
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IQVIA
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Reading,
United Kingdom
...
making the CRA role more efficient and discussions at site more productive. Next generation clinical ... contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International
...
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IQVIA
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Bucharest,
Romania
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Join us in our exciting journey!!
IQVIA is looking for a Clinical Research Associate to ... .
Minimum of 1 year of experience as a CRA.
Experience in using CTMS, eTMF and EDC systems
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IQVIA
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Vienna,
Austria
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Join IQVIA as a enior Clinical Research Associate / Sr CRA (m/w/d) home-based throughout Austria in our single sponsor department , and advance your career in clinical research. You’ll enjoy
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