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IQVIA
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Amsterdam,
Netherlands
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Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery.
Essential Functions
• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team
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IQVIA
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Amsterdam,
Netherlands
...
maintaining standard statistical requirements in data analysis tools and templates, ensuring compliance with ... SAS or R programming.
Working knowledge of relevant regulatory requirements (e.g., GCP, ICH) and
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IQVIA
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Breda,
Netherlands
...
)**
Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and
...
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IQVIA
-
Amsterdam,
Netherlands
...
)**
Assist Clinical Research Associates (CRAs)/In-house Clinical Research Associate (iCRA) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and
...
-
IQVIA
-
Amsterdam,
Netherlands
...
maintenance of clinical trials, whilst enabling compliance with regulatory requirements.
• Assist with the ... successfully deliver the agreed project scope in compliance with sponsor requirements and/or the RSU Management
...
