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Chapel Hill

    Senior Clinical Research Coordinator - Chapel Hill, United States - University of North Carolina at Chapel Hill

    University of North Carolina at Chapel Hill
    University of North Carolina at Chapel Hill Chapel Hill, United States

    1 week ago

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    Description

    A global higher education leader in innovative teaching, research and public service, the University of North Carolina at Chapel Hill consistently ranks as one of the nation's top public universities.

    Known for its beautiful campus, world-class medical care, commitment to the arts and top athletic programs, Carolina is an ideal place to teach, work and learn.


    One of the best college towns and best places to live in the United States, Chapel Hill has diverse social, cultural, recreation and professional opportunities that span the campus and community.


    University employees can choose from a wide range of professional training opportunities for career growth, skill development and lifelong learning and enjoy exclusive perks for numerous retail, restaurant and performing arts discounts, savings on local child care centers and special rates on select campus events.

    UNC-Chapel Hill offers full-time employees a comprehensive benefits package, paid leave, and a variety of health, life and retirement plans and additional programs that support a healthy work/life balance.

    Primary Purpose of Organizational Unit

    The UNC School of Medicine has a rich tradition of excellence and care. Our mission is to improve the health and wellbeing of North Carolinians, and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education, and research.

    We strive to promote faculty, staff, and learner development in a diverse, respectful environment where our colleagues demonstrate professionalism, enhance learning, and create personal and professional sustainability.

    We optimize our partnership with the UNC Health System through close collaboration and commitment to service.


    OUR VISION
    Our vision is to be the nation's leading public school of medicine.

    We are ranked 2nd in primary care education among all US schools of medicine and 5th among public peers in NIH research funding.

    Our Allied Health Department is home to five top-ranked divisions, and we are home to 18 top-ranked clinical and basic science departments in NIH research funding.


    OUR MISSION
    Our mission is to improve the health and well-being of North Carolinians and others whom we serve. We accomplish this by providing leadership and excellence in the interrelated areas of patient care, education, and research.

    Patient Care:

    We will promote health and provide superb clinical care while maintaining our strong tradition of reaching underserved populations and reducing health disparities across North Carolina and beyond.


    Education:

    We will prepare tomorrow's health care professionals and biomedical researchers by facilitating learning within innovative curricula and team-oriented interprofessional education.

    We will cultivate outstanding teaching and research faculty, and we will recruit outstanding students and trainees from highly diverse backgrounds to create a socially responsible, highly skilled workforce.


    Research:
    We will develop and support a rich array of outstanding health sciences research programs, centers, and resources. We will provide infrastructure and opportunities for collaboration among disciplines throughout and beyond our University to support outstanding research. We will foster programs in the areas of basic, translational, mechanistic, and population research.

    Position Summary

    This position will serve as a Senior Clinical Research Coordinator within the Dr.

    Joseph Muenzer MPS Research & Treatment Center (Muenzer MPS Center) in the Division of Genetic and Metabolism, Department of Pediatrics.

    The Muenzer MPS Center is focused on improving the outcomes of individuals with mucopolysaccharidosis (MPS) and their families and developing new treatments.

    The Muenzer MPS Center team is dedicated to developing new treatments for children and adults with MPS, a group of ultra rare genetic disorders, including clinical trials to test new forms of intravenous enzyme replacement therapy as well as novel therapies, such as gene therapy and intrathecal drug delivery.

    The Muenzer MPS Center (Director Dr. Joseph Muenzer) offers an exciting opportunity for a Clinical Research Specialist to become an integral part of this fast growing and successful team. You will work directly with the PIs (Dr. Joseph Muenzer and Dr.

    Elizabeth Jalazo) and with the MPS Clinical Research Director (Lindsay Torrice, CPNP) on our clinical trials delivering novel therapeutics to children/adults with MPS and other lysosomal storage disorders.

    This is a highly rewarding job working with our interdisciplinary and collaborative team of physicians, advanced practice providers, research staff, and dedicated health professionals, who love working with children and adults with rare genetic disorders and are dedicated to improving their health and quality of life.


    The Senior Clinical Research Coordinator is responsible for the planning, organization, conduct, and evaluation of multi-faceted clinical research protocols, including study execution, developing strategies and solutions to improve study processes and execution, providing reviews of other team members' work product, and serving as mentor and subject matter expert.

    Minimum Education and Experience Requirements


    Bachelor's degree in a discipline related to the field assigned and one year of related training or experience; or equivalent combination of training and experience.

    All degrees must be received from appropriately accredited institutions.

    Required Qualifications, Competencies, and Experience


    • Strong verbal and written communication skills with ability to clearly, concisely, professionally, and effectively communicate in writing and verbally with staff, faculty, and individuals in other organizations.
    • Must be able to work and communicate with diverse populations effectively and professionally.
    • Ability to work independently as well as function as part of a team.
    • Proficient with Microsoft Outlook, Excel, and Word.
    • Clinical research experience in Phase I, II and/or Phase III clinical trials.
    • Knowledge of clinical research and the fundamentals of regulatory practices relevant to clinical research.
    • A demonstrated ability to work independently with limited guidance.
    • Demonstrated leadership experience and strong organizational skills.
    • Ability to identify needs and develop and implement improvements.
    • Experience in study start-up activities, including development of source documentation, working with external vendors and internal units/departments to ensure compliance with protocol and applicable regulations.
    Preferred Qualifications, Competencies, and Experience


    • Preference will be given for previous experience with therapeutic clinical research involving drugs/medications for mucopolysaccharidoses.
    • Experience in preparing regulatory submissions, interacting with local and central IRBs
    • Working knowledge of medical terminology, techniques and methodologies used in developing, coordinating, and managing clinical research projects (including the ability to extract medical information and summarize patient data.)
    Special Physical/Mental Requirements Campus Security Authority Responsibilities

    Not Applicable.

    Special Instructions Quick Link
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