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IQVIA
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Parsippany, New Jersey
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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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Parsippany, New Jersey
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and close-out visits) in accordance with contracted scope of work and Good Clinical Practice ... .
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol
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IQVIA
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Parsippany, New Jersey
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Role Overview: As a Clinical Research Associate, you’ll be at the forefront of ensuring our ... , monitoring, and close-out visits, ensuring compliance with Good Clinical Practice (GCP) and International
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IQVIA
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Parsippany, New Jersey
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IQVIA is seeking a Senior Clinical Research Associate with at least 2 years of monitoring ... requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
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IQVIA
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Parsippany, New Jersey
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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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Parsippany, New Jersey
...
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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Parsippany, New Jersey
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quality and integrity of site practices – escalating quality issues as appropriate
Managing progress ... colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research
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