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    Associate Clinical Trial Manager - London, United Kingdom - Medpace, Inc.

    Medpace, Inc.
    Medpace, Inc. London, United Kingdom

    Found in: Jooble UK O C2 - 3 days ago

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    Description

    Medpace is currently seeking candidates with CVRM PhDs and/or Post-Doctoral Research experience for a full-time, office-based Associate Clinical Trial Manager (aCTM) to join our London Clinical Trial Management team.

    The aCTM will be a part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities.

    Candidate must have a desire to transfer and apply analytical and academic skills in clinical project administration and management.

    A fantastic opportunity for recent PhD graduates to enter the industry, receive solid foundational training, work in an international environment, and develop their career in the research and development of cutting-edge therapeutics .

    Candidates should expect to have an intensive training period and show the desire and aptitude for an accelerated career path into Clinical Trial Management (CTM).

    working closely with the project coordinator and clinical trial manager
    Compile and maintain project-specific status reports within the clinical trial management system
    Interact with the internal project team, Sponsor, study sites, and third-party vendors
    Provide oversight and quality control of our internal regulatory filing system
    Create and maintain project timelines
    Coordinate project meetings and produce quality minutes
    PhD in Life Sciences
    cardiomyopathy, Lipid disorders, obesity, heart failure, endocrinology, NASH, acute coronary syndrome, CVD, preventive cardiology
    Fluency in English with solid presentation skills
    Prior experience within the CRO or pharmaceutical industry not required but will be advantageous
    Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

    Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach.

    We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

    Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.
    Hybrid work-from-home options (dependent upon position and level)
    Competitive PTO packages
    Company-sponsored employee appreciation events
    Employee health and wellness initiatives
    Flexible work schedule
    Competitive compensation and benefits package
    Structured career paths with opportunities for professional growth
    Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility
    EO/AA Employer M/F/Disability/Vets
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