Clinical Trial Manager - Reading, Berkshire, United Kingdom - IQVIA Argentina

    IQVIA Argentina
    IQVIA Argentina Reading, Berkshire, United Kingdom

    Found in: Jooble UK O C2 - 1 week ago

    Default job background
    Part time
    Description

    IQVIA's cFSP (sponsor-dedicated) team are seeking a Clinical Trial Manager to join us on our mission to drive healthcare forward.

    The Clinical Trial Manager will partner with the Clinical Trial Assistants, Clinical Research Associates, Central Trial Managers and Global Trial Managers to ensure overall study delivery at country level.

    Partner with global, local country teams and study team to provide high level country strategy, drive study progress and country level study delivery.

    (Plan, manage, and maintain oversight of clinical study execution in accordance with the global program strategy, through leadership of the cross-functional Local Study Team (LST)
    Support country-level operational planning and accountable for site selection within assigned country(ies)
    monitoring plan, study specific training documents.
    Contribute to, deliver and/or lead CRA, Investigator and Study Coordinator training
    Oversight and monitoring of applicable vendor activities e.g., laboratories and equipment provisioning
    Contribute to the study-level forecast for investigational product, support study level accountability and reconciliation across assigned countries, management of ELE (enrolment long-range estimates) process
    Monitor the execution of the clinical study against timelines, deliverables, and budget for that country:
    Monitor and review country and study trends Review Monitoring Visit Reports
    Conducts on-site quality visits with CRAs where/when appropriate and supports the maintenance of investigator site relationships
    Bachelor's degree in a healthcare or other scientific discipline
    Minimum 1-2 years' experience of leading local/regional or global teams
    Minimum 1-2 years' clinical trial project management experience
    CROs, central labs, imaging vendors, etc.).
    Local knowledge / expertise of regulatory environment, study start up process and associated timelines etc.
    Clinical trial processes and operations
    Project and Program management including oversight of study deliverable, budgets and timelines
    Time, cost and quality metrics, Key performance indicators (KPIs)
    #IQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.