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  • Posted: May 26, 2026
    Deadline: Not specified
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    IQVIA, formerly Quintiles and IMS Health, Inc.,is an American multinational company serving the combined industries of health information technology and clinical research. It is a provider of biopharmaceutical development and commercial outsourcing services, focused primarily on Phase I-IV clinical trials and associated laboratory and analytical services,...
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    Associate Clinical Data Manager

    Job Overview

    • We are seeking an experienced and detail-oriented Associate Lead Data Manager to oversee data management activities across multiple clinical projects. In this role, you will ensure high-quality data delivery in line with sponsor requirements, while collaborating with cross-functional teams, sites, and external partners.

    Key Responsibilities

    • Gather study set-up requirements through effective communication with stakeholders.
    • Lead database set-up, configuration, and validation to ensure optimal study design and data integrity.
    • Support validation and implementation of new device integrations.
    • Perform ongoing data cleaning activities to ensure accurate, timely, and high-quality deliverables.
    • Ensure all outputs meet established quality standards and client expectations.
    • Train and mentor new team members.
    • Lead internal study meetings, participate in sponsor meetings, and support audits and study kick-offs.
    • Track and manage project progress, identify risks, and implement corrective actions in collaboration with the Data Team Lead (DTL).
    • Oversee database revisions and support the adoption of new technologies.
    • Collaborate with programming teams to drive process improvements and automation initiatives.
    • Ensure compliance with all required training and electronic SOPs (eSOPs).
    • Contribute expertise to the development, review, and maintenance of standard operating procedures (SOPs) and work instructions.
    • Maintain effective, collaborative communication with leadership, line managers, and cross-functional teams.

    Qualifications & Requirements

    • Education: Master’s degree in Life Sciences / Postgraduate in Science / Bachelor of Pharmacy or equivalent preferred.
    • Strong understanding of the drug development lifecycle and overall clinical research processes.
    • Proficiency in English (spoken and written).
    • Advanced skills in Microsoft Office applications (Excel, Word, Outlook).
    • Strong analytical, organizational, and problem-solving abilities.
    • Excellent communication and stakeholder management skills.
    • Ability to manage multiple projects and meet deadlines in a fast-paced environment.

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    Method of Application

    Interested and qualified? Go to IQVIA on iqvia.wd1.myworkdayjobs.com to apply

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