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    PS Clinical Research Coord - Salt Lake City, United States - University of Utah

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    Open Date 04/22/2024 Requisition Number PRN38333B Job Title PS Clinical Research Coord Working Title PS Clinical Research Coord Job Grade E FLSA Code Administrative Patient Sensitive Job Code? Yes Standard Hours per Week 40 Full Time or Part Time? Full Time Shift Day Work Schedule Summary

    Monday to Friday: 9:00 AM -5:30 PM, occasional weekend and after hours required.

    VP Area U of U Health - Academics Department Pediatric Administration Location Campus City Salt Lake City, UT Type of Recruitment External Posting Pay Rate Range $47,650-$68,349 Close Date Open Until Filled Yes Job Summary


    The Department of Pediatrics at the University of Utah School of Medicine has an immediate opening for a Clinical Research Coordinator.


    This position coordinates the implementation, quality control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives.

    Oversees research studies in an administrative and operational capacity while maintaining compliance with guidelines set by governing agencies.

    Examples of responsibilities include, interfacing with patients and families, obtaining informed consents, supervising data collection, and entering study data in electronic databases.

    And mentoring junior staff.

    The University of Utah offers a comprehensive benefits package, a wellness program, and competitive salary commensurate with experience. Mutual respect and appreciation are highly valued within the University of Utah.

    Responsibilities


    • Oversees compliance to protocol; manages quality control, completion and submission of study related documentation; prepares reports for organizations and agencies.
    • Develops study budgets; monitors budget expenses and billing for allied services; negotiates payment schedule with sponsor and fees for internal services.
    • Monitors enrollment goals and initiates strategies to promote enrollment and participant compliance. Coordinates and performs responsibilities related to research participants including determining subject population availability, developing informed consents and screening materials, screening and recruiting subjects, scheduling visits, obtaining informed consent, answering subject inquiries, overseeing study visits and acting as a liaison between participants and study-related parties.
    • Recognizes, tracks and reports adverse events and protocol deviations.
    • Prepares for and coordinates site visits made by sponsors or federal agencies during course and at the close of the study.
    • Represents the research program at meetings, national and international research consortia.
    • Prepares, submits and maintains IRB, FDA, NCI, NIH, NSF and/or other regulatory documents and research correspondence.
    • Contributes to developing educational materials and educates the community and other research professionals regarding studies and related research issues.
    • Supervises, mentors and trains new junior or student research staff.
    • Coordinates with referring physicians to provide information regarding available research projects and to maintain a strong referral basis.
    • Develops and maintains patient databases, investigational logs and records of drugs administered, medical devices monitored and/or procedures followed.
    • Assists the Principal Investigator in the development of study protocols.
    • Assures proper laboratory samples are collected and results are reported to the proper entities.
    • Completes ongoing training on techniques of clinical research coordination and practices, FDA Good Clinical Practices (GCP), and clinical research standard operating procedures to ensure compliance with policy and procedure, research sponsors and Federal rules and regulations.
    Disclaimer


    This job description has been designed to indicate the general nature and level of work performed by employees within this classification.

    It is not designed to contain or be interpreted as a comprehensive inventory of all duties, responsibilities and qualifications required of employees assigned to the job.

    Comments

    Work Environment and Level of Frequency that may be required:


    Nearly Continuously:
    Office environment.


    Seldom:
    Infectious disease, oils (there is air or skin exposure to oils or other cutting fluids).

    Physical Requirements and Level of Frequency that may be required:


    Nearly Continuously:
    Hearing, listening, talking.


    Often:
    Repetitive hand motion (such as typing), walking, standing, sitting.


    Seldom:
    Bending, reaching overhead.


    The staff member must be able to demonstrate the knowledge and skills necessary to provide care appropriate to the age of the patients served on his or her assigned unit.

    The individual must demonstrate knowledge of the principles of life span growth and development and the ability to assess data regarding the patient's status and provide care as described in the department's policies and procedures manual.

    Minimum Qualifications


    Bachelors degree in a health sciences or related field or equivalency (one year of education can be substituted for two years of related work experience) with two years professional research experience and completion of University RATS Clinical Certification within one year of hire required.

    Exceptional organizational skills, attention to detail, and demonstrated human relations and effective communication skills also required.


    Knowledge of Good Clinical Practices, FDA, HIPAA and IRB regulations; an understanding of research procedures; and the ability to function independently is preferred.

    Departments may require IRB CITI Course or IATA DGR training within a specified timeframe.


    Departments may prefer a nursing degree for this position, which requires the incumbent to have two years related experience and possess a nationally recognized research compliance certification.

    This position is patient-sensitive and must fulfill all associated requirements.

    We protect our patients, coworkers and community by requiring all patient-sensitive employees to be immunized according to CDC standards and hospital policy.

    Limited exemptions may be made for documented medical contraindications or religious beliefs that object to vaccinations.


    Applicants must demonstrate the potential ability to perform the essential functions of the job as outlined in the position description.

    Preferences


    • Completion of ACRP or SOCRA certification within one year of eligibility
    Type Benefited Staff Special Instructions Summary Additional Information

    The University is a participating employer with Utah Retirement Systems ("URS").

    Eligible new hires with prior URS service, may elect to enroll in URS if they make the election before they become eligible for retirement (usually the first day of work).

    Contact Human Resources at for information.

    Individuals who previously retired and are receiving monthly retirement benefits from URS are subject to URS' post-retirement rules and restrictions.

    Please contact Utah Retirement Systems at or or University Human Resource Management at if you have questions regarding the post-retirement rules.

    This position may require the successful completion of a criminal background check and/or drug screen.


    The University of Utah values candidates who have experience working in settings with students and patients from all backgrounds and possess a strong commitment to improving access to higher education and quality healthcare for historically underrepresented students and patients.

    All qualified individuals are strongly encouraged to apply. Veterans' preference is extended to qualified applicants, upon request and consistent with University policy and Utah state law. Upon request, reasonable accommodations in the application process will be provided to individuals with disabilities.


    The University of Utah is an Affirmative Action/Equal Opportunity employer and does not discriminate based upon race, ethnicity, color, religion, national origin, age, disability, sex, sexual orientation, gender, gender identity, gender expression, pregnancy, pregnancy-related conditions, genetic information, or protected veteran's status.

    The University does not discriminate on the basis of sex in the education program or activity that it operates, as required by Title IX and 34 CFR part 106.

    The requirement not to discriminate in education programs or activities extends to admission and employment.

    Inquiries about the application of Title IX and its regulations may be referred to the Title IX Coordinator, to the Department of Education, Office for Civil Rights, or both.


    To request a reasonable accommodation for a disability or if you or someone you know has experienced discrimination or sexual misconduct including sexual harassment, you may contact the Director/Title IX Coordinator in the Office of Equal Opportunity and Affirmative Action (OEO/AA).

    More information, including the Director/Title IX Coordinator's office address, electronic mail address, and telephone number can be located at:

    Online reports may be submitted at

    This report includes statistics about criminal offenses, hate crimes, arrests and referrals for disciplinary action, and Violence Against Women Act offenses.

    They also provide information about safety and security-related services offered by the University of Utah.

    A paper copy can be obtained by request at the Department of Public Safety located at 1658 East 500 South.

    Posting Specific Questions

    Required fields are indicated with an asterisk (*).


    • Do you have a related Bachelor's degree or equivalency? (2 years related work experience may be substituted for 1 year of education)
    • Yes
    • No
    • Please indicate the number of years of professional research experience that you have:
    • Less than 1 year
    • 1 year or more, but less than 2 years
    • 2 year or more, but less than 4 years
    • 4 years or more, but less than 6 years
    • 6 years or more
    • Are you certified as a Clinical Research Professional? (CCRP, CCRC, or CCRA)
    • Yes
    • No
    Applicant Documents

    Required Documents


    • Resume
    Optional Documents


    • Cover Letter
    • Appropriate discharge document (such as a DD-21- Member Copy 4) - Veteran Only - Call
    • Addendum to the University of Utah - Veteran Only - Call after submission


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