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    Senior Clinical Research Assistant - Baltimore, United States - University of Maryland, Batlimore

    University of Maryland, Batlimore
    University of Maryland, Batlimore Baltimore, United States

    4 days ago

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    Description

    The University of Maryland, Baltimore (UMB) Marlene & Stewart Greenebaum Comprehensive Cancer Center (UMGCCC) has an opening for a Senior Clinical Research Assistant.

    This position is the primary interface, along with the faculty member for cancer patients enrolled in clinical trials.

    This position is responsible for coordination of screening, enrolling, and consenting the patients and subsequently guiding the patient through the research protocol, their courses of care/medication, research visits, data collection, standard of care issues and direct research support.

    This position works directly with the medical care team, ancillary hospital staff, the Sponsor, and data managers in the Cancer Center.

    This is a full-time exempt position that will work Monday through Friday. Some schedule flexibility may be required.

    UMB employees are strongly encouraged to follow all CDC recommendations related to COVID-19 vaccinations and booster doses.

    Employees whose job duties require them to work in clinical settings or at clinical or field sites continue to be subject to the vaccine requirements of those sites.

    For additional information on protocols and exemptions, please visit the COVID-19 website.


    Benefits:
    UMB offers a comprehensive benefits package that prioritizes wellness, work/life balance, and professional development.

    Exempt regular staff receive a generous leave package that includes over 4 weeks of vacation accrued each year, paid holidays, unlimited accrual of sick time, and comprehensive health insurance and retirement options; professional learning and development programs; tuition remission for employees and their dependents at any University System of Maryland school; and flexible work schedules and teleworking options (if applicable per job).


    Essential Functions:

    • Responsible for facilitating and coordinating clinical research patient visits and data collection. Supports the conduct of clinical trials, including the coordination of start-up activities, scheduling and preparing for patient visits, assisting with data collection and clarification, and general administrative duties.
    • Assists in the preparation of Institutional Review Board (IRB) and Health Insurance Portability and Accountability Act (HIPPA) protocol development and ensure compliance of research operations with protocols. May assist in developing and recommending policies and procedures and/or design methods for clinical research activities.
    • Coordinates data collection of the research study including obtaining medical records, lab results, diagnostic results, visit notes, etc. Coordinates recruitment and screening subjects for research studies according to IRB approved protocols. May communicate directly with study participants.
    • Coordinates paperwork for submission of IRB protocol, IRB amendments, and IRB continuing reviews. Document and report all adverse events as appropriate. Participates in audits and monitor visits as needed according to policy.
    • Performs the coordination of data analysis and interpretation and develops statistical reports of study data using descriptive statistics using SAS, STATA, and SPSSS software. Assists in developing, submitting, and providing content or grants, papers, abstracts, manuscripts, and presentations. Conducts and analyzes literature searches. Develops and establishes a database to track research data.
    • Coordinates development of research protocols and materials by providing study analysis and forming conclusions and recommendations.
    • Documents in accordance with state and federal standards pertaining to specific research participants enrolled in the study. Maintains communication with participants and colleagues regarding protocol specific information and research orders. Provides assessments and ensure protocol compliance while participants are in a study.
    • Performs other related duties as assigned.

    Education:
    Bachelor's degree in a scientific field of study related to the research of the clinical setting.

    Experience:
    Two (2) years of experience in clinical research in research being performed in unit.

    Other:
    May consider a combination of directly related experience and education.


    Knowledge, Skills, and Abilities:
    Knowledge of position requirements. Knowledge of all applicable requirements, regulations, and laws. Skill in effective use of applicable technology/systems. Ability to effectively communicate both verbal and written thoughts, ideas, and facts. Ability to work cooperatively with others and independently.

    Ability to demonstrate, understand, apply, and adhere to the UMB Core Values of Accountability, Civility, Collaboration, Diversity, Excellence, Leadership, and Knowledge.


    Hiring Range:
    Low to mid-$50,000s, commensurate with education and experience.

    UMB is an Equal Opportunity/Affirmative Action Employer.

    All qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected Veteran status, age, or any other characteristic protected by law or policy.

    For assistance related to employment, please contact the Staffing department at


    If you anticipate needing a reasonable accommodation for a disability under the Americans With Disabilities Act (ADA), during any part of the employment process, please submit a UMB Job Applicant Accommodation Request.

    You may also contact Please note that only inquiries concerning an ADA request for reasonable accommodation will be responded to from this email address.

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