PK/PD Documentation Specialist (m/w/d)
Deliver high quality coordination of the centralized support by the document service management group for upload of relevant Clinical Pharmacology & Pharmacometrics (CPP) documents (e. g. population PK/PD data transfer plans, population PK/PD analysis plans and population PK/PD reports) within the required regulatory system per global aligned procedures of client. Perform memo and report strawman support, document quality control (QC), prepare Clinical Pharmacology & Pharmacometrics documents for submission or health authority interactions, provide writing support, implement QC process refinement as defined by the Clinical Pharmacology & Pharmacometrics organization, and track the operational progress amongst stakeholders. Services are delivered by applying organizational and scientific writing skills to support document writing and QC in line with applicable guidelines and regulations.
Responsibilities
Education and Experience Requirements/Qualifications:
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
- Informații detaliate despre oferta de muncă
Firma: IQVIA Localiția: Bucureşti
Bucharest, Bucharest, RomaniaAdăugat: 17. 7. 2025
Postul de muncă activ
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