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    Clinical Research Coordinator - Seattle, United States - Seattle Institute for Biomedical and Clinical Research

    Seattle Institute for Biomedical and Clinical Research
    Seattle Institute for Biomedical and Clinical Research Seattle, United States

    3 weeks ago

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    Description
    Seattle Institute for Biomedical and Clinical Research
    Seattle Institute for Biomedical and Clinical Research

    Clinical Research Coordinator - Feemster/Donovan

    Seattle Institute for Biomedical and Clinical Research

    Clinical Research Coordinator - Feemster/Donovan
    Seattle, WA 98108


    Title:
    Clinical Research Coordinator

    Job Class:
    Hourly/Non-Exempt - $30-36/hour


    DOE

    PI:
    Laura Feemster, MD, MS; Lucas Donovan, MD

    Summary:


    The Clinical Research Coordinator will work as a key team member on a series of pulmonary studies based at the VA Puget Sound Health Care System Center of Innovation, including trials sponsored by the American Lung Association Airways Clinical Research Centers (ACRC) and the Patient-Centered Outcomes Research Institute (PCORI) see below for links to these studies.

    This position requires an individual who understands the principles of scientific investigation and clinical trials and is capable of in-depth understanding of the study protocol.

    The candidate must possess strong scientific, organizational, and interpersonal skills. The position is full-time, Monday through Friday, with potential for hybrid in-person/telework after a training period. Salary will be based according to

    the applicants research experience and includes benefits

    and 403b retirement plan.

    Responsibilities may include:
    Lead recruitment, screening, enrollment, consent, and follow-up of clinical trial participants according to study protocols, including:

    reviewing medical charts
    conducting study visits
    administering questionnaires
    measuring participant vital signs including height, weight, and blood pressure
    timely and accurate data entry
    preparing participant mailings
    tracking study activities
    conducting and transcribing qualitative interviews

    In our role as a data coordinating center for a large multi-site trial

    facilitate clinical site training
    monitor site activities, including data quality and adverse events, providing feedback as necessary
    maintain/modify paper- and electronic data capture forms
    maintain/modify manual of procedures and disseminate to sites
    maintain compliance with applicable IRB, human subjects and data security guidelines and regulations

    Develop and maintain study databases and files
    Prepare written applications and reports
    Prepare/distribute meeting agendas and notes
    Develop and maintain a study budget

    Required Knowledge and Experience:
    BA/BS in scientific or health related field
    2+ year experience management of human subjects research
    Outstanding organizational and communication skills
    Keen attention to detail
    Ability to work in a collaborative team environment
    Research compliance regulations
    Microsoft applications including Outlook, Word, Excel, and Access

    Prefer Knowledge and Experience with:
    Electronic medical record systems
    Electronic data capture systems, e.g. REDCap, Qualtrics
    Applicants who submit a cover letter highlighting experience and interest will receive preference
    If you have any questions about the application process, please email
    Diversity enriches research and promotes the best healthcare. We are committed to building and sustaining an equitable and inclusive environment.

    We encourage individuals whose backgrounds or interests align with this commitment, as well as individuals from all backgrounds that are underrepresented in research, to apply.

    Currently, only US Citizens, Permanent Residents, Green Card holders with proper work documents and F-type Visa holders may apply.
    SIBCR Pays 100% (less $90/month) for Employees and 75% of Dependent Premiums per month.
    Offered to all employees working 20+ hours per week on a regular basis:
    Medical and Prescription Insurance
    Vision Insurance
    Life Insurance, Short Term Disability and Long Term Disability
    Employee Assistance Program
    403(b) Retirement Plan with pre-tax and Roth options with Matching Contribution (up to 2.5%) plus Non-Match Contribution of 5%
    Sick Leave - accrues at 1 hour for 20 paid hours
    Vacation Leave - accrues at 1 hour for 20 paid hours
    11 Paid Holidays + one personal holiday
    ORCA transportation pass at a nominal monthly fee
    Other mandated leave such as FMLA and WA PFML
    Voluntary Benefits include Flexible Spending Account, AFLAC, Voluntary Term Life
    No other types of compensation offered at this time

    Equal Employment Opportunity Policy:


    The Seattle Institute for Biomedical and Clinical Research does not discriminate in employment on the basis of race, color, religion, sex (including pregnancy), gender identity or status as transgender, national origin, caste, political affiliation, sexual orientation, marital status, disability, genetic information, age, membership in an employee organization, retaliation, parental status, military service, or other non-merit factor protected by federal, state or local law.


    Accessibility:
    If you need an accommodation as part of the employment process please contact Human Resources at

    Email:


    Equal Opportunity Employer, including disabled and veterans.

    If you want to view the

    Know Your Rights:
    Workplace Discrimination is Illegal poster, please choose your language:

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