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    Clinical Trial Manager - London, United Kingdom - Medpace

    Medpace
    Medpace London, United Kingdom

    Found in: Jooble UK O C2 - 2 days ago

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    Description

    Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in the United Kingdom, specifically in London and Stirling.

    Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of expertise or to expand to a new therapeutic area .

    We provide remote flexibility only with relevant experience (after probation). We offer a very competitive salary/bonus program, plus equity grants which have become very lucrative for our associates.

    Manage and provide accountability for day-to-day operations of the project, as defined by the contract and according to ICH/GCP and all other applicable laws, rules, and regulations
    Serve as primary Sponsor contact for operational project-specific issues and study deliverables
    Provide cross-functional oversight of internal project team members and deliverables, which includes ensuring all necessary project-specific training is provided
    Review and provide input for study protocol, edit check specifications, data analysis plan, and final study report, when applicable
    Develop operational project plans
    Manage risk assessment and execution
    Manage site quality, including direct supervision of project Clinical Research Associates and monitoring deliverables

    Bachelor's degree in a health or life science-related field; Advanced degree in a health or life science-related field preferred;
    Minimum of 2 years of Clinical Trial Management experience, CRO experience preferred;
    5+ years of Project Manager/Clinical Trial Manager experience at a CRO required for a remote-based role;
    Management of overall project timeline;
    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 #J-18808-Ljbffr
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