IQVIA is seeking an EDC Clinical Trial Designer to create high quality data collection tools for new trials and to support the design, development, documentation, testing and implementation of clinical eCRF databases.
The role involves designing eCRF forms using Oracle InForm/Central Designer or Veeva CDMS/Studio, ensuring SOPs and CDISC/CDASH/SDTM standards are applied to deliver a quality product on time. A BA/BS and at least 2 years in CDM are required.
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Clinical EDC Trial Designer - Data & eCRF Specialist in Livingston employer: IQVIA Argentina
IQVIA is an excellent employer that fosters a collaborative and innovative work culture, providing its employees with the opportunity to grow professionally while working on impactful financial reporting across Europe. With a strong emphasis on employee development and proficiency in leading financial systems like PeopleSoft and SAP, team members can expect meaningful career advancement in a supportive environment that values integrity and excellence.
