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    Syngene Clinical Trials Jobs | Apply Now for Project Associate Position

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    Syngene Clinical Trials Jobs | Apply Now for Project Associate Position

    Are you looking for an exciting career in clinical research? Syngene International Limited, a global leader in discovery, development, and manufacturing services, is inviting applications for the role of Project Associate – Clinical Trials in Bangalore. This role offers the opportunity to support clinical trial operations, ensure regulatory compliance, and contribute to world-class research projects with top pharmaceutical and biotechnology clients.

    About Syngene:

    Founded in 1993, Syngene International Ltd. is a global discovery, development, and manufacturing organization providing integrated scientific services to industries including pharmaceuticals, biotechnology, nutrition, animal health, consumer goods, and specialty chemicals. With a team of over 4,240 scientists, Syngene partners with global leaders such as Bristol-Myers Squibb, Baxter, Amgen, GSK, Merck KGaA, and Herbalife to enhance R&D productivity, reduce costs, and accelerate innovation.

    Job Details

    • Job Post: Project Associate, Clinical Trials
    • Location: Bangalore, India
    • Department: Clinical Operations
    • Education: Master’s degree in Life Sciences or Pharmacology.
    • Experience: 1–3 years in clinical research within Clinical Operations.
    • Technical Skills: Knowledge of ICH-GCP, Indian regulatory guidelines, SOP development, Microsoft Office tools, and handling audits.
    • Behavioral Skills: Proficiency in English, integrity, and strong organizational ability.

    Job Purpose:
    The Clinical Trial Assistant plays a vital role in maintaining study-specific documentation and supporting the smooth execution of clinical trials.

    Key Responsibilities:

    • Support Clinical Project Managers and Clinical Research Associates by updating and maintaining clinical systems to track site compliance and project timelines.
    • Assist in preparing, handling, distributing, filing, and archiving clinical documentation and reports.
    • Manage clinical trial supplies, case report forms (CRFs), queries, and data flow.
    • Serve as the central point of contact for communications and documentation across project teams.
    • Coordinate with Quality Assurance during in-house audits and with translation agencies for study document translation.
    • Provide administrative support and ensure the timely submission of timesheets.

    Equal Opportunity Employer:

    Syngene is committed to equal employment opportunities and provides a supportive workplace for all, including reasonable accommodations for individuals with disabilities.

    APPLY ONLINE HERE

    Keywords: Syngene International Limited, Project Associate Clinical Trials, Bangalore, Clinical Research Jobs, Clinical Operations Careers, ICH-GCP Compliance, Job Posting

    Apply now

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