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    Clinical Research Coordinator - Summerville, United States - Articularis Healthcare

    Articularis Healthcare
    Articularis Healthcare Summerville, United States

    2 weeks ago

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    Description

    Job Description

    Job DescriptionSalary:

    Articularis Healthcare Group (AHG) is currently seeking a full-time Clinical Research Coordinator in our Summerville, SC location.

    Our Benefits:

    4-day work week

    Benefits package that includes group medical, dental, vision, short-term & long-term disability insurance, paid holidays, PTO and 401K.

    Our Company:

    Articularis Healthcare Group, Inc (AHG) is a physician led and owned organization dedicated to improving healthcare by supporting independent rheumatology practices across the country. As the nation's largest rheumatology specialty group with 20+ practices across 7 states, AHG provides access to best business practices, advisory and management services, and value-based treatment pathways.

    Please visit our website at for more information.

    Our Mission:

    Delivering the highest quality community-based rheumatology services with a commitment to patient care, physician leadership and excellence.

    The Position:

    Articularis Healthcare Group is seeking to add an experienced Clinical Research Coordinator (CRC) to our Summerville, SC. The candidate will work closely with our team of physicians and research coordinators to help execute Rheumatology clinical trials at our Summerville, GA office.

    As a Clinical Research Coordinator, a typical day might look like:

    • Coordinating and managing multiple investigational study protocols. The CRC will assume a primary role in:
    • Reviewing, comprehending and developing a familiarity with the investigational study protocols
    • Conducting or participating in the informed consent process with study participants
    • Screening and enrolling eligible study participants in an efficient and timely manner
    • Performing study procedures in accordance with GCP and OSHA guidelines (lab draws/processing, vital signs, EKG, subcutaneous injections, dispense study medications, manage and monitor the use of study electronic devices, etc.)
    • Collecting data and documenting procedures as required by the protocol. Assuring timely completion of Case Report Forms, query resolution, and database lock deadlines.
    • Preparing and submitting IRB reports and maintaining regulatory documents compliance with the help of the Clinical Research Regulatory Coordinator (including but not limited to: serious adverse events, protocol deviations, screening logs, database updates, and annual renewal reports)
    • Maintaining all study records in accordance with sponsor requirements and facility policies.
    • Maintaining effective and ongoing communication with sponsor, research participants and investigators during the study.
    • Coordinating and preparing for monitor / audit visits
    • Working effectively and cooperatively with colleagues to provide back-up coordination as required
    • Maintaining adequate inventory of study supplies
    • Assisting with orientation of new employees.
    • Other duties including travel to Investigator meetings

    This job might be for you if:

    • You have a bachelor's degree in chemistry, biology, or other natural, life or health care science and at least one year of strong, investigational drug studies experience. An associate degree and three years of strong, relevant research experience may be substituted for the required experience.
    • You have 1+ years of experience in a Clinical Research Coordinator role.
    • You have knowledge of clinical research terminology, research documentation, informed consent process, regulatory / IRB submission, and Good Clinical Practice (GCP)
    • You have a proven track record of detail-orientation and high level of performance and accuracy.
    • You have the ability to work well independently and effectively within a team dynamic. Conduct daily operations with minimal supervision and maintain a flexible work schedule.
    • You have the ability to multi-task and set priorities against deadlines.
    • You have the ability to exercise judgment and discretion. Strong critical thinking and problem solving.
    • You have the ability to effectively communicate, both written and verbally
    • You have strong computer software knowledge and skills
    • You have excellent interpersonal skills and professional demeanor
    • You have patience, compassion, enthusiasm, and a strong desire to help humankind through advances in clinical research

    You should apply if:

    • Assertive, self-motivated, passionate and able to learn new things
    • Accountable, takes ownership of projects, follow-up and follow through
    • Success driven through personal pride
    • Commitment to personal and professional excellence
    • Team player. Understands quality and produces efficiency and repeatable quality work.
    • Learns from mistakes. Follows directions well
    • Willing to give and accept positive criticism/feedback without being defensive.
    • Must be efficient and conscientious in delivering medical care to patients.
    • Must have awareness of patient confidentiality

    Next Steps:

    Once you submit your application, a member of our Talent Acquisition Team will review your resume and application. A team member will reach out to you directly if you are a fit for the position.

    EEO/AA-M/F/disabled/protected veteran

    *Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions

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