The Sr. CDM will lead and contribute to data management activities in support of Client's studies across all stages of clinical drug development. Summary of Key Responsibilities - Contribute to data management activities as a lead study data manager in support of Client's clinical studies - Lead database build activities including leading cross-functional review of eCRF content, review of edit check specifications, and perform user acceptance testing - Monitor data collection, coding, and clean…
Szczegóły oferty
Firma
IQVIA
Lokalizacja
Warszawa, mazowieckie
Kategoria
Unknown
Data publikacji
20.06.2025
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