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    Clinical Research Associate - 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

    The Clinical Research Associate at Medpace is offering the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them.

    For those with medical and/or health/life science interest and background who want to explore the research field, travel the UK, and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you Please note that to take full advantage of the training on offer, you must be within commuting distance of our Medpace central London office.

    Our successful Clinical Research Associates possess varied backgrounds in medical and other science-related healthcare fields. Pharmaceutical/Device Sales Representatives
    Biotech Engineers
    PhD/Pharm.
    Health and Wellness Coordinators
    Site Coordinators, Clinical Research Coordinators
    Research Assistants.
    PACE – MEDPACE CRA TRAINING PROGRAM
    Through our PACE Training Program, you will join other P rofessionals A chieving C RA E xcellence:

    PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.

    To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

    This role takes you on a journey through travel and excitement which will allow you to make a difference on a large scale through the enhancement of pharmaceuticals and medical devices.

    Work within a team of therapeutic and regulatory experts
    Defined CRA promotion and growth ladder with potential for mentoring and management advancements
    Competitive pay and opportunity for significant travel bonus
    Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
    Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
    Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
    Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
    Regulatory document review;
    Medical device and/or investigational product/drug accountability and inventory;
    Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
    Assessing the clinical research site's patient recruitment and retention success and offering suggestions for improvement;

    Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance.

    Minimum of a bachelor's degree; Health or life science related field preferred;
    Willing to travel approximately 60-80% nationally;
    Familiarity with Microsoft Office; 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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