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    Job · 12543910

    Voiant logo

    Clinical Coordinator I - Ophthalmology

    Voiant · Remote · remote · Posted 64d ago

    ₹7.0L - ₹12.0L PA2–5 yrsfulltimeSourced fromNaukri

    About a minute. You'll make an account on the way through.

    About this role

    RESPONSIBILITIES & ACCOUNTABILITIES

    • Provides entry level administrative support to assigned Project Manager(s), as well as site management for all assigned clinical trials.
    • Administratively assists with all assigned project activities, ensures protocol adherence, and addresses non-compliance issues, as appropriate.
    • Partners with clinical sites to coordinate and execute site activation procedures, personnel training, equipment credentialing, and query resolution.
    • Looks for and identifies trends or issues with site activities and escalates appropriately.
    • Ensures sites have adequate training and arranges ad hoc training(s) with the appropriate subject matter experts when necessary to ensure ongoing quality imaging and standardization.
    • Responsible for updating internal databases with accurate subject status and information in a timely manner.
    • Pulls weekly reports and trackers from internal databases as requested.
    • Responsible for maintaining Clinical Trial Records and performing scheduled assessments in a timely manner.
    • Responsible for timely filing all project documentation and key correspondence for assigned trials.
    • Responsible for study closeout record e-transfer transfer/shipments
    • Assists PM with the coordination of internal, sponsor and other meetings, as needed and upon request.
    • Creates study specific draft documentation, as well as weekly meeting agendas and minutes for PM.
    • May provide administrative support during project-related audits.
    • Assists with all other departmental requests as needed and upon request.

    EDUCATION & EXPERIENCE

    • 1-2 years administrative support experience, or similar, required.
    • Clinical Trial experience or knowledge a plus
    • Proficient in Microsoft Word, Excel, PowerPoint, and experience using database software
    • Excellent organizational skills and attention to detail
    • Strong written and verbal communication skills
    • Proactive and ability to work independently.
    • Flexible and able to manage multiple priorities and deadlines.
    • Positive attitude, ability to work within a team environment.


    Sourced from naukri

    Skills

    ClinicalRegulatory AffairsOphthalmologyclinical trial

    Clinical Coordinator I - Ophthalmology · waiting for your command