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ICF manages the USAID-funded Surveys for Monitoring in Resilience and Food Security (SMRFS) project as part of Feed the Future, the U.S. Government’s flagship initiative to reduce global hunger and improve food security.
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ICF is a world leader in global health and our work helps partner countries to strengthen the following: 1) the quality of the data they use to inform key health policy decisions; 2) the information systems they use for detection and surveillance of infectious diseases including tuberculosis; and 3) the monitoring and evaluation programs they implement to evaluate important health and development programs.
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Bring your strong interpersonal and organizational skills to the forefront as you oversee the Trial Master File and contribute to ICF and protocol development in collaboration with the project management team.
$30.55 - $44.3 an hourFull-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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The On-Call/Temporary Archaeologist will assist ICF archaeologists primarily in fieldwork, with tasks including construction monitoring, survey, testing, evaluation, and data recovery. On-Call employees may work concurrent projects outside of their ICF assignment (as long as their outside work does not create a conflict of interest with the work they do for ICF.
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The CRC B (Regulatory Coordinator) will assist with preparing and processing regulatory documents through the IRB and other research review boards and have the ability to handle a variety of clinical trial related regulatory responsibilities in accordance with University of Pennsylvania, GCP, ICF, and FDA guidelines.
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Contribute meaningfully during internal audits and external monitoring visits including: Evans Class Monitors, Quality Trust, HRLA, DOH, PCR, DDS, DDA in the District of Columbia. To ensure that the program is operated in compliance within the Scope of Work, Volunteers of America Chesapeake's policies and procedures, licensing and ICF/ Medicaid waiver regulations.
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Manage the creation and maintenance of critical study documents assigned to Clinical Development (e.g., Clinical Trial Protocols (CTPs), Investigator’s Brochures (IB), Informed Consent Forms (ICF), Risk-Based Medical Monitoring Plan, Clinical Study Reports (CSRs), regulatory documents) with high quality and consistency with CDP, TPP and AskBio SOPs.
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Provide all necessary leadership and guidance to keep the quality of clinical study-related documents (clinical study protocol (PRT), investigator's brochure (IB), clinical study report (CSR), medical monitoring plan (MMP), safety management plan (SMP), informed consent form (ICF), clinical study data listing/table and regulatory agency/IRB submission document); oversee, write and/or review clinical study-related documents listed above.
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The Regulatory Specialist will serve as a regulatory liaison to internal and external investigators, sponsors, collaborating divisions, departments and institutions, and Institutional Review Boards (IRBs), Data Safety and Monitoring Boards, Biosafety committees, Laboratory facilities, and external regulatory agencies.
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Contribute to safety sections of clinical study documents including Study Protocols, Informed Consent Forms (ICF), Statistical Analysis Plans (SAP), Medical Monitoring Plans (MMP), Clinical Study Reports (CSR), IB Reference Safety Information (RSI), Summary of Clinical Safety (SCS), Integrated Clinical Safety (ICS), Publications, Manuscripts, and other relevant documents.
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Independently perform environmental compliance monitoring at construction sites (including preconstruction clearance surveys and environmental awareness training), coordinating with construction crews, and being responsive to ever-changing schedules.
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Collaborates on and supports CTM/Sr. CTM on required tasks prior to commencement of clinical trials that include, but are not limited to: clinical planning, protocol development, case report form (CRF) development, IRB submissions, investigator agreements, informed consent form (ICF) development, site selection, Trial Master File structure and preparation, and communication with clinical trial sites regarding administrative documentation, support materials and training.
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Description The On-Call/Temporary Archaeologist will assist senior archaeologists primarily in fieldwork, with tasks including survey, testing, evaluation, data recovery, and construction monitoring.
$48,364 - $82,218 a yearPart-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Provide post-operative, routine or preventative medical treatments and interventions as per MD or RN order (i.e., G-tube feedings, wound and skin care, urinary drainage systems maintenance, blood glucose monitoring, passive and active range of motion therapy.
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Responsible for the scientific and clinical inputs and review of study-related documents and analysis plans, including protocols, investigative brochures, informed consent forms (ICF), case report forms (CRF), associated data management documents, statistical analysis plans (SAP), independent Data Monitoring Committee (IDMC) and/or Study Review Committee (SRC) charters, and clinical study reports (CSR.
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