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Dr. Amanda-Jensen-Doss, a faculty member in the University of Miami’s Department of Psychology, is seeking a new post-baccalaureate research assistant to support an NIMH-funded research study focused on identifying key indicators of fidelity to measurement-based care, utilizing coding of therapy session recordings and analysis of digital user data from a measurement feedback system.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Assist assigned Clinical Research Coordinator with the creation and/or review of study flowsheets to ensure study is conducted according to protocol requirements. Perform study events and collects clinical data as directed by principal investigator and protocol.
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Reviews protocol specimen processing requirements and ensures that an adequate inventory of necessary supplies are available or ordered and delivered prior to study start and throughout study conduct.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Assist with preparation of protocol revisions and reports to the IRB and National Institutes of Health (NIH). Responsibilities will primarily center on coordinating the coding of study therapy tapes, assisting in database construction, managing undergraduate research assistants, overseeing IRB submissions and updates, and project administrative tasks.
ExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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To ensure study data is collected to a high quality in accordance with ICH-GCP, protocol and lab manual. Attends all pre-study meetings, including SIVs and protocol trainings for assigned studies.
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Reviews protocol and provides study feasibility input to the NCH-RI Leadership and Study Start-up Team. Works with QI/QA team to ensure quality standards are being met and reports adverse events, protocol deviations.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Provide study support from protocol and budget development to submission and completion for Phase IV as well as Investigator Initiated Trials (IITs) Doctorate degree (DVM, MD, PhD, or PharmD) in biological sciences.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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This role assists in the day-to-day operations of clinical research protocol implementation and carries out study coordination duties from protocol initiation to study close-out according to regulatory/sponsor guidelines.
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Serves as the central resource within the Research Development Center to provide authoritative expertise and regulatory guidance on complex issues including but not limited to protocol development, and multi-site activation and study maintenance.
Full-timeRemoteExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Works collaboratively with study team members, regulatory and operational staff to develop or coordinate the development of the study design and protocol required information. Advises and assists the Investigator, key study personnel, and other team members in the development of data tools, record keeping, study budget, process improvement plans, and efficient timelines for research studies; coordinates the ongoing analysis and modification of protocols; and recommends amendments to study protocols as appropriate.
Full-timeRemoteExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Substantial clinical study protocol experience, as lead author, required. Under minimal supervision, the Medical Writer will critically evaluate, analyze, and interpret the medical literature to select primary resource materials for adequate study design, statistical significance, scientific rigor and absence of bias.
Full-timeRemoteExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Coordinates and executes the collection, compilation, and analysis of clinical research data from studies conducted by PIs and study teams at Nicklaus Children's and the NCH-RI. Interacts with patients and families to recruit study subjects and ensures compliance with protocol guidelines and requirements of regulatory agencies.
Full-timeExpandApply NowActive JobUpdated 2 days ago - UpvoteDownvoteShare Job
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Provide coaching to junior staff for study-level documents as well as submission-level documents and ensure all staff comply with company standard operating procedures (SOPs) and training requirements.
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Provides nursing-related care to clinical trial study participants as outlined (and applicable) in the study protocol. Interacts with patients and families to recruit study subjects and ensures compliance with protocol guidelines and requirements of regulatory agencies.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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The Budget Analyst Associate will have overall responsibility for creation of study budgets based on detailed knowledge of the study protocol requirements, additional guidance from the sponsor, and input from assigned key staff.
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protocol study jobs in Miami, FL
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