Clinical Data Specialist

2 weeks ago


Bloemfontein, Orange Free State, South Africa IQVIA Argentina Full time

Job Summary:

We are seeking a highly skilled Clinical Data Associate to join our team at IQVIA Argentina. As a Clinical Data Associate, you will be responsible for performing comprehensive data management tasks, including data review, query generation, and resolution. This role requires strong analytical and problem-solving skills, as well as excellent communication and collaboration abilities.

Key Responsibilities:

  • Data Management: Perform comprehensive data management tasks, including data review, query generation, and resolution.
  • Data Reconciliation: Perform ongoing data reconciliation of all data streams.
  • Meetings and Communication: Attend study-related meetings and teleconferences, and provide timely status updates to the DM and DMLs as needed.
  • Study Closeout: Perform Study Closeout/Archiving Activities, including QC of subject/site Archival CRFs.
  • Reporting: Create and provide status/metric reports, and generate reports on EDC and track cleaning progress.
  • eCRF Management: Manage Freeze/Lock of eCRF and file documentation in the virtual Trial Master File (TMF).

Requirements:

  • Education and Experience: Bachelor's degree in a Health or Science discipline with experience in clinical research. Data Management experience and experience working on a clinical trial are mandatory.
  • Skills and Qualifications: Knowledge of current industry standards (e.g., CDISC, SDTM, CDASH, etc.) for Advanced CDA. Project management skills, vendor management skills, and proficiency with Microsoft Office tools are also required.


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