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    Clinical Research Coordinator - Santa Ana, United States - Clemente Clinical Research

    Clemente Clinical Research
    Clemente Clinical Research Santa Ana, United States

    3 weeks ago

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    Description

    Job Description

    Job Description

    Job Description:

    As the experienced Clinical Research Coordinator Manager at Clemente Clinical Research, you will work with a team that is dedicated to bringing quality care to those in the community who need it most. The majority of our patients are Hispanic, speak Spanish, and are diabetic. We work mostly in the diabetic wound care space, where we help patients find access to new treatments and devices so they can avoid amputations. The patients we support and provide care to are from underserved and minority populations that typically don't get the focus they deserve. We are on a mission to fix that.

    Visit our website to learn more about our mission:

    As a member of the Clemente team, you will::

    • Oversee our team of clinical research coordinators
    • Oversee the five active trials and additional trials coming in the new year
    • Work closely with renowned doctors and researchers
    • Work with our doctors across multiple clinics to recruit, screen, and enroll patients
    • Review and comprehend all study protocols
    • Coordinate and attend monitor site visits and prepare site visit documentation
    • Ensure study staff is properly trained on trial protocols
    • Oversee patient scheduling and follow-up activities
    • Facilitate and coordinate the daily clinical trial activities
    • Manage and maintain documentation for each trail
    • Collect protocol data and enter information into the electronic data capture (EDC) system
    • Act as a reviewer to ensure the trial protocols are being followed accurately
    • Works with monitors to ensure protocol guidelines and deadlines are being met

    Experience we are looking for:

    • 5+ years as a Clinical Research Coordinator (CRC)
    • Experience in wound care and diabetes (not required)
    • Fluent in English and Spanish
    • Phlebotomy certificate
    • Experience in patient-facing roles
    • Experience in IRB submissions, source documentation, and trial management
    • A thorough understanding of regulatory requirements and principles of GCP

    Clemente Clinical Research Summary:

    Who are we?

    We're doctors, researchers, and advocates for better health services, education, and resources. We like to think of Clemente as a safe haven where community members can receive the most advanced healthcare available. A joint effort between everyone involved, Clemente ensures everything we do is done ethically, efficiently, and with the utmost respect for the well-being of participants.

    What do we do?

    In a nutshell, we do clinical research for phase I-IV trials. This means, we take promising advances in medicine and implement them in our patient care, testing their effectiveness and benefits. What makes us different, is our goal to make conducting and participating in clinical research accessible and enjoyable. We're dedicated to medical progression and improving healthcare outcomes, but we're also committed to delivering the highest level of service and support to our clients and study participants.

    How do we do it?

    Think of Clemente as the expert curator who assembles the best team to conduct each clinical trial. We carefully select the most qualified researchers, doctors, and participants to administer the most ethical, efficient, and respectful clinical trials focused on the well-being of participants.

    Who are we here for?

    Specifically, we're here for individuals in underserved communities. We're advocates for better health services, education, and resources, and it's these community members that need our support. More broadly, Clemente is here for sponsors, clinical research organizations, and doctors as we work together to achieve meaningful improvements and better treatments for all. But, it's our participants who inspire, motivate, and keep the work moving forward.

    Company DescriptionWe invite doctors, researchers, and community members to join us in our deep commitment to serving our underserved communities by ensuring that they have access to high-quality clinical research. Together, we can make a lasting impact by empowering our communities, enhancing healthcare outcomes, and unlocking the potential for a healthier future. We hope to create a world where access to high-quality clinical research is a reality for all. We have found immense joy in the process and know that you will, too.

    Company Description

    We invite doctors, researchers, and community members to join us in our deep commitment to serving our underserved communities by ensuring that they have access to high-quality clinical research. Together, we can make a lasting impact by empowering our communities, enhancing healthcare outcomes, and unlocking the potential for a healthier future. We hope to create a world where access to high-quality clinical research is a reality for all. We have found immense joy in the process and know that you will, too.\r
    \r
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