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IQVIA
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Oslo,
Norway
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Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for complex projects and programs
RESPONSIBILITIES
Acts as
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IQVIA
-
Oslo,
Norway
...
Prepares and/or reviews regulatory documents to support clinical trial submissions. Independently provides regulatory support for more complex projects.
RESPONSIBILITIES
Acts as a
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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 ... .
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and
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IQVIA
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Oslo,
Norway
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and milestone deliverables. Comply with Good Clinical Practices (GCPs), applicable regulatory ... Good Clinical Practices and relevant regulatory guidelines
Excellent communication, interpersonal
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IQVIA
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Oslo,
Norway
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protocol for scientific/regulatory soundness and feasibility, identification of target site and principal ... current knowledge of scientific, clinical, regulatory, commercial and competitive landscape in Cardiology
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