Full-Time Research Professional - Durham - beBeeClinicalResearchAssociate

    beBeeClinicalResearchAssociate

    Job title: Clinical Research Associate, Full Service

    Description
    Job Overview

    We are seeking a skilled professional to perform monitoring and site management work. The ideal candidate will ensure that sites conduct the study(ies) and report data as required by the study protocol, applicable regulations, and sponsor requirements.

    In this role, you will perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements (i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines).

    Responsibilities:

    • Perform site monitoring visits to ensure compliance with GCP/ ICH regulations;
    • Work with sites to adapt subject recruitment plans in line with project needs;

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