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  • Posted: Feb 21, 2026
    Deadline: Not specified
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  • Sharing a Vision to Drive Healthcare Forward Healthcare is an industry designed to help humans. As a global community, we continuously invest and commit to advancing human health. To deliver value and real outcomes. To rise to the challenge to find the next breakthrough by making the most of increasingly limited resources. We are inspired by the potential ...
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    Data Acquisition Expert (eSource Specialist) (m/w/d) - Homebased - Bellville

    Job Summary:

    • We are seeking a highly skilled Data Acquisition Expert (eSource Specialist) to join our team. The ideal candidate will be responsible for acquiring Electronic Health Record (EHR) and integrating it with Electronic Data Capture (EDC) system to automate data entry processes. This role requires a deep understanding of FHIR-based EHR data, EDC systems, and clinical trial processes.

    Key Responsibilities:

    • Acquire and analyze EHR/EMR data for integration with EDC systems.
    • Ensure site readiness and study preparedness for integration.
    • Collaborate with study teams to update eCRF forms as per integration requirements.
    • Assess whether studies are in production or need deployment to production.
    • Conduct analysis to determine migration needs and identify relevant fields and forms.
    • Prepare detailed integration specification documents.
    • Maintain outstanding knowledge of EDC systems and familiarity with FHIR and EHR data.
    • Understand clinical trial processes, standards, and study design.
    • Adapt quickly to new technologies and methodologies.
    • Solve complex problems efficiently.
    • Communicate effectively with team members and stakeholders.
    • Coordinate cross-functional activities between different teams to ensure seamless integration and data flow.

    Requirements

    • Minimum of 5 years’ experience managing data in support of clinical research.
    • Proven experience in data acquisition and integration, particularly with EHR/EMR and EDC systems.
    • Strong knowledge of EDC and study design.
    • Understanding of clinical trial processes and standards.
    • Excellent problem-solving skills and ability to adapt quickly.
    • Knowledge of study design and clinical research methodologies.
    • Outstanding communication skills, both written and verbal.
    • Ability to work collaboratively in a team environment.

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    Method of Application

    Interested and qualified? Go to IQVIA on jobs.iqvia.com to apply

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