University of Maryland, Baltimore (UMB) is currently seeking a Senior Clinical Research Assistant to join the School of Medicine - Orthopaedics. The selected candidate will be responsible for screening, consenting, and enrolling participants in research studies. The position will complete baseline and follow-up data collection with participants and using data from the medical record. The individual will be responsible for entering data, assisting with data clean-up, and maintaining that all research studies are being conducted according to IRB approved protocols. The position will also assist with IRB responsibilities as needed. Performs other duties as assigned. * *BENEFITS (Contractual/C2 Employee): UMB offers a comprehensivebenefits packagethat prioritizes wellness, work/life balance, and professional development. Contingent Category II staff receive a generous leave package that includes over 2 weeks of vacation each year, paid holidays, personal leave, sick time, and time for community service; subsidized comprehensive health insurance and supplemental retirement options; professional learning and development programs; limited tuition remission for employees enrolled at UMB; life insurance and long-term disability; and flexible work schedules and teleworking options (if applicable per job). UMB is Ranked Among the Best Employers for Diversity by Forbes 2022 & 2023. /_//_/ /_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. This position is required to be vaccinated against COVID−19. For additional information on protocols and exemptions, please visit the _//COVID-19 website//_._// / * *PRIMARY DUTIES: * Responsible for facilitating and coordinating clinical research patient visits and data collection. The position will support 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. * Assist 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. * Assists in developing, submitting, and providing content for 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 participant 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 duties as assigned. MINIMUM QUALIFICATIONS: 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. Supervisory Experience:N/A. Certification/Licensure:N/A. Other:May consider a combination of directly related experience and education. * *KNOWLEDGE, SKILLS, 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 Respect and Integrity, Well-being and Sustainability, Equity and Justice, and Innovation and Discovery. * *HIRING RANGE:$53,000 - $56,000 per year (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 atHRJobs@umaryland.edu. 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 aUMB Job Applicant Accommodation Request. You may also contactHRDiversity@umaryland.edu. Please note that only inquiries concerning an ADA request for reasonable accommodation will be responded to from this email address. *Job: Reg or CII Exempt Staff *Organization: School of Medicine - Orthopaedics *Title: *Senior Clinical Research Assistant Location: null Requisition ID: 240000KL