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    Sr. Clinical Research Associate - Los Angeles, United States - Worldwide Clinical Trials

    Worldwide Clinical Trials
    Worldwide Clinical Trials Los Angeles, United States

    5 days ago

    Default job background
    Description
    Who We Are

    We're a global, midsize CRO that pushes boundaries, innovates, and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe.

    It is built by those who take pioneering, creative approaches and implement them with quality and excellence.
    What Clinical Operations Site Management Does At Worldwide

    Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve.

    These roles are the backbone of every strong CRO, helping drive breakthrough scientific research and playing a lead role on every clinical trial.

    All CROs will promise you growth, opportunity and maybe even a challenge. But we offer more than that. We offer an uncommon experience – one you can't get anywhere else, with a team unlike anyone else.
    At Worldwide we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up.

    We empower our team members to treat every trial like a patient's life depends on it – because it does.

    Our leaders are in the trenches with you daily - committed to advancing science and moving mountains for our customers.

    What You Will Do

    Responsible for managing the research activities at sites participating in Worldwide's clinical research projects, which are predominantly late phase (II-III).

    Conduct all types of visits – site qualifications, initiation, monitoring, site management and close out visits.
    Ensure adherence and compliance with Good Clinical Practices (GCPs) and applicable local and international regulations and Standard Operating Procedures (SOPs)
    assure timely submission of data, including appropriate reporting and follow-up for all safety events by site personnel

    What You Will Bring To The Role
    Excellent interpersonal, oral, and written communication skills in English
    Superior organizational skills with attention to details
    Ability to work with little or no supervision
    Proficiency in Microsoft Office, CTMS and EDC Systems

    Your Experience
    Bachelor's Degree or a Nursing Degree required
    Experience with Phase II-III Oncology experience preferred
    Ability to meet the travel requirements of the job. Our metrics are 6-8 days on site per month.

    Why Worldwide
    At Worldwide, we balance fun with the serious business of changing lives. We have a values-driven culture that is built from the ground up.

    We empower our team members to treat every clinical trial like a patient's life depends on it – because it does.

    Our leaders are in the trenches with you - committed to advancing science and moving mountains for our customers.
    #UncommonCRO
    #J-18808-Ljbffr
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