Key Accountabilities: Clinical Trial Site Activation - Initiate and coordinate activities and essential documents management during start up towards the compilation of a high quality Investigator Initiation Package (IIP) leading to approval for site initiation - Provide support to resolve issues or concerns and timely escalation of site issues where applicable - Prepare, validate and submit regulatory documents such as completed IIP, Institutional Review Board (IRB) approval forms, FDA 1572/Att…
Szczegóły oferty
Firma
Parexel
Lokalizacja
Polska
Kategoria
Unknown
Data publikacji
11.08.2025
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