Clinical Research Coordinator, Sealy Center on Aging (Partial Remote) **Galveston, Texas, United States** **New** Clerical & Administrative Support UTMB Health Requisition # 2402330 **Minimum Qualifications:** Bachelor's degree or equivalent, and two years of directly related experience. **Job Description:** The Clinical Research Coordinator obtains human subject data for clinical research activities via methods specified in the study protocol and performs general administrative duties supporting the study. **Job Duties:** + Applies knowledge in contributing to Good Clinical Practice (GCP) activities and/or other regulatory activities. + Schedules, coordinates, and participates in the pre-site visit and site initiation visits; coordinates study initiation. + Maintains and monitors source documentation and appropriate forms as per protocol for quality and accuracy, including participant records; assists with the quality assurance process. + Incorporates directions from other health care disciplines into clinical research protocols when reviewing patient eligibility; assists in eliciting relevant data from sources outside of the hospital. + Conducts behavioral intervention visits in the clinic setting. + Develops and maintains productive working relationship with the study monitor; attends and participates in campus coordinator workshops. + Identifies and recruits clinical research subjects for participation of studies, collects data, and monitors enrollment goals. + Work with research databases to collect milestone research visits and develop reports. RED Cap database knowledge a plus. + Mentors new clinical research coordinators and assistant clinical research coordinators. + Assists with grant/protocol preparation and submission to IRB, OCR or OSP under direction of research coordinator under the direction of the PI and with answering IRB stipulations to obtain final approval; documents IRB approval and contract approval + Knowledgeable of IRB practices e.g., submitting a protocol amendment, protocol deviation, and continuing review. + Under direction of PI may draft various communications with Sponsor and/or regulatory documents to be sent to the Sponsor. + May assist PI and/or research nurse coordinator in the planning and design of source documents for protocol. + Assists in developing procedures for data collection and storage. + Assists in processing and sharing data per data use agreements or if indicated asper regulations.Experience working with outside reporting agencies such as CROMS orclinicaltrials.gov a plus. + Assists in precepting new clinical research staff and educating other research staff regarding scientific aspects of studies. + Assists with the budget development; may monitor ledgers. + Adheres to internal controls established for department. + May assist PI in obtaining Informed Consent from study participant and documents appropriately. + Adheres to internal controls and reporting structure. + If appropriately trained and tested for competency, obtains Vital Signs and performs phlebotomy; monitors participants’ labs and notifies the PI of laboratory findings + May attend and participate in the Investigator meeting + Performs related duties as required. **Salary Range:** Commensurate with Experience **Equal Employment Opportunity** UTMB Health strives to provide equal opportunity employment without regard to race, color, religion, age, national origin, sex, gender, sexual orientation, gender identity/expression, genetic information, disability, veteran status, or any other basis protected by institutional policy or by federal, state or local laws unless such distinction is required by law. As a VEVRAA Federal Contractor, UTMB Health takes affirmative action to hire and advance women, minorities, protected veterans and individuals with disabilities. Compensation