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IQVIA
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Livingston,
United Kingdom
...
assays and associated pipelines across all service areas in the business (i.e. Laboratory Ops, Quality
...
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IQVIA
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Glasgow,
United Kingdom
...
requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH
...
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IQVIA
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Cambridge,
United Kingdom
...
requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH
...
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IQVIA
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London,
United Kingdom
...
requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH
...
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IQVIA
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Bath,
United Kingdom
...
requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH
...
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IQVIA
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Reading,
United Kingdom
...
requirements.
• i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH
...
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IQVIA
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Reading,
United Kingdom
...
interest for the client, as part of ‘peer to peer’ engagement (i.e., beyond IQVIA capability presentations
...
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IQVIA
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London,
United Kingdom
...
interest for the client, as part of ‘peer to peer’ engagement (i.e., beyond IQVIA capability presentations
...
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IQVIA
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London,
United Kingdom
...
.
The UK&I Value and Access capabilities are centred on Market Access strategic advice aligned to field ... &I Value & Access Consulting is a critical function within in the Market Access and Patient
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IQVIA
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Leeds,
United Kingdom
...
, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e
...
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IQVIA
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Reading,
United Kingdom
...
, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e
...
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IQVIA
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Reading,
United Kingdom
...
domain of Biotech, providing customized Phase I through IV services globally, and offering expertise ... clinical process (PH I – IV).
Solid understanding of commercialization and the principles of drug
...
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IQVIA
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London,
United Kingdom
...
domain of Biotech, providing customized Phase I through IV services globally, and offering expertise ... clinical process (PH I – IV).
Solid understanding of commercialization and the principles of drug
...
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IQVIA
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Reading,
United Kingdom
...
activities in Phases I through IV of standard to high complexity and priority ≥ 3 years of recent
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IQVIA
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London,
United Kingdom
...
contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International
...
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IQVIA
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Reading,
United Kingdom
...
, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e
...
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IQVIA
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Reading,
United Kingdom
...
clinical research regulatory requirements, i.e. Good Clinical Practice
• (GCP) and International
...
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IQVIA
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Reading,
United Kingdom
...
contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International
...
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IQVIA
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Reading,
United Kingdom
...
, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e
...
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IQVIA
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London,
United Kingdom
...
programming team
In-depth knowledge of applicable clinical research regulatory requirements, i.e. Good
...
