Saturday, June 20

    Dutch Speaking Associate Centralized Monitor x1

    • Company: IQVIA
    • Location: Bloemfontein, South Africa (office-based)
    • Employment Type: Full-time
    • Salary: R1,529,598 per annum
    • Language Requirement: Fluent in Dutch
    • Other Locations: Additional locations may be available
    • Posted: 2026

     Job Overview

    The Associate Centralized Monitor supports clinical project teams by performing centralized monitoring, administrative tasks, data review, and system updates. The role ensures compliance with SOPs, ICH-GCP guidelines, and regulatory requirements while helping maintain data integrity and study quality across clinical sites.

     Main Purpose

    To provide centralized monitoring and project support for clinical studies, ensuring study timelines, data quality, and compliance standards are met, while assisting in administrative and technical tasks related to clinical trial management.

     Key Responsibilities

    • Complete all required training and adhere to SOPs and quality standards.

    • Provide administrative support: generate reports, maintain trackers, prepare status updates, and follow up on outstanding items.

    • Update and maintain study systems and ensure alignment with project timelines.

    • Prepare i-Site Packs and other study documentation.

    • Perform centralized monitoring activities and assess site/data quality.

    • Monitor site performance metrics and address missing data, SDV backlogs, and visit schedules.

    • Identify site-level risks and track corrective actions.

    • Conduct Subject Level Data Review (SLDR) and escalate issues as necessary.

    • Support study-specific analytics and trend analysis.

    • Manage access tasks and coordinate with vendors when required.

    • Serve as backup for Centralized Monitors/Senior Centralized Monitors.

    • Support technical tools, including Excel formulas, macros, and tool design.

    • Maintain effective communication with clinical sites, CRAs, and internal teams.

     Minimum Qualifications

    • Bachelor’s or postgraduate degree in Life Sciences or related field.

    • At least 1 year of experience in clinical research or centralized monitoring (preferred).

    • Fluent in Dutch (mandatory).

    • Proficient in MS Office, particularly Excel.

    • Strong communication, organizational, and problem-solving skills.

    • High attention to detail and data accuracy.

    • Ability to work effectively with cross-functional teams and external sites.

     Company Overview

    IQVIA is a leading provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries worldwide. They focus on accelerating the development and commercialization of innovative medical treatments to improve patient outcomes.

    • Committed to integrity in hiring and zero tolerance for candidate fraud.

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