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The onsite (at UTMB Galveston main campus) Study Coordinator - Regulated Studies is responsible for assisting the Study Director with all aspects of the study, including pre-study, in-life, and reporting phases of a study.
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Manage activities related to study committees (CEC, DSMB/DMC, Independent Medical Monitor) or overseeing third party management of committee activities per study SMP and associated Charters.
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The Medidata Rave Study Builder will be responsible for creating Rave studies for therapeutic oncology trials. Incumbent will bring experience with study build activities in Medidata Rave, preferably in oncology.
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Conduct ongoing medical reviews of safety related events (e.g., AEs, DD/DMs) per study SMP. Manage accurate and timely safety related regulatory reporting (AEs, SAEs, UADEs) per study and regulatory requirements including collaboration with regulatory affairs and clinical operations, or overseeing activities of third-party managing safety reporting.
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The School Psychologist will work consistently and creatively to meet the needs of all students, be responsible for academic advising and student socialization, collaborate on the Child Study Team, and partner with School Leaders and campus-based Special Education teams to provide related professional development to teachers and staff.
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Responsible for project management of a clinical study from protocol development up to Clinical Study Report (CSR) completion and Trial Master File (TMF) archiving. Report important study performance information, including study start-up metrics, enrolment, data collection timelines/quality.
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The Center coordinates the John Belk International Program (study abroad), international student services, and other international initiatives. Manage all aspects of faculty-led study abroad programs working closely with faculty, the Assistant Director for Global Experiences, Executive Director of International Education, program partners, and service vendors.
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PROFESSIONAL REQUIREMENTS Possess a Bachelor’s degree in Civil/Environmental Engineering or related engineering field Have 6-10 years of increasingly-responsible, professional experience in the study, design, and construction administration of water, wastewater and stormwater collection and conveyance infrastructure and related facilities water distribution/transmission and gravity sewer pipelines, force mains, and pump stations.
$83,000 - $128,000 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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CIEE is a non-profit study abroad and intercultural exchange organization that transforms lives and builds bridges between individuals and nations through study abroad and international exchange experiences that help people develop skills for living in a globally interdependent and culturally diverse world.
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Masters degree from an accredited institution in a field of study related to horticulture or crop science, and/or related to apple production must be earned by date of hire. Persons with a Ph. D. from an accredited institution in a field of study related to horticulture, or crop science with a background in apple production.
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Ensures Trial Master File (TMF) is maintained throughout the study and helps with periodic TMF QC/audits. The Clinical Research Associate (CRA) will independently manage all clinical aspects of a small to medium-sized clinical study or, with supervision, assume significant management responsibilities on a large-scale study.
Full-timeExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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Prepares and submits Institutional Review Board (IRB) documents (i.e., Schedules study-related meetings and training sessions and provides instruction to study team for specific study assignments; educates staff regarding scientific aspects of study and trains ancillary staff regarding clinical studies or trials; Manages research study inventory and supplies (such as medications, equipment, devices) and maintains required compliance documentation.
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Liaises with study website developer, develops study recruitment materials and advertisements, manages study recruitment advertisement campaigns. Leads execution & control of a biomedical &/or social science project or research study.
$49,850 - $70,419 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
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Leads and/or participates in the development and review of study documents including CRF design, project plans, Service Provider Oversight plans, TMF (Trial Master File) plan. Manages study sites and study related activities including but not limited to site feasibility, selection, start up, subject recruitment, enrollment, study management, monitoring report review, site management, trial master files, and data review / clean up.
Full-timeExpandApply NowActive JobUpdated 6 days ago
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