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The Document Management Analyst (DMA) role works closely with the Department of Justice, Health Care Fraud Division attorneys in a fast-paced setting and assist in the investigation and prosecution of various matters to enforce the laws of the United States, up to and including support assistance for witness interviews, deposition preparation, and in-courtroom trial support.
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The New Jersey Judiciary consists of: the Supreme Court, the Superior Court including the Appellate Division and the Trial Court of the 15 vicinages in New Jersey, the Tax Court and the Municipal Court System.
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This position offers an exciting opportunity to engage in professional legal work, leveraging your expertise and trial skills in tasks such as interviewing witnesses, preparing trial dockets, trying misdemeanor bench trials and prosecuting criminal cases in Wichita Municipal Court.
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Confirm archival and inspection readiness of all Clinical Technology Trial Master File (TMF) documents. Experience integrating other clinical trial modules (e.g.: lab, safety, IRT, coding etc.,) with the EDC system.
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The Senior Clinical Trial Manager is accountable for delivery of selected and/or regional activities within a trial (e.g., manage and oversee vendor deliverables, collaborate with functions to set up activities [e.g., DM, IRT, and eRT], support site activation and recruitment, support data review/cleaning activities, support PI/ICF development.
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Overview:The role will serve as the “TMF Archivist” and support trial-specific clinical oversight of the TMF as established within Genmab’s procedural documents, GCP-ICH guidelines, and regulatory health expectations during the conduct and closure of the trial.
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Produces forensic reports pertaining to juvenile competency to stand trial, transfer of cases to criminal court, allocation of parental rights (custody/visitation issues), juvenile diagnostic assessments, and children's services adult mental health assessments.
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Responsible for managing relationships with CROs and other vendors for all study activities including study start-up, close out, and completion of Trial Master File. Responsible for initial RFP obtainment and contributes to CRO/vendor selectionResponsible for setting up, negotiating, and monitoring Task Order invoice payments for CRO (direct service and pass through costs); as well as oversee scope change negotiations.
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The Senior Scientist plays an integral role in the development and hands-on execution of critical projects that support the Heme Translational Medicine Department's aims in translational science, clinical trial support, and pre-clinical drug development.
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Monitor fund activities on an ongoing basis and reconcile fund balances upon clinical trial closure by working with MGH Cardiology financial leaders and Grant Accounting to ensure timely account closure.
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The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent process.
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Oversee the collection and management of clinical trial documentation to be filed in the Trial Master File (TMF). CTM, Clinical trial, Phase I-III, oncology, drug development, CRO, FDA, ICH Guidelines, GCP, TMF.
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The Director provides Good Clinical Practice (GCP) guidance and best-practice expertise to facilitate optimal clinical trial execution compliance management as it relates to Process Deviations and CAPA management to and ensure study adherence to applicable GCP regulations throughout all phases of clinical development.
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Incumbents must possess or obtain Law Enforcement Officer certification through the Utah State Peace Officer Standards and Training (POST) Agency during the probationary period for new hires or the trial period for promoted County employees.
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Experience in Family Court trial-level representation is also desirable. In the area of parent representation, the Appellate Attorney will help fulfill ILS’s statutory mission to “make efforts to improve the quality of services provided pursuant to article 18-B of the county law” by working in consultation with others to develop training programs, creating templates and other resources, and providing individual consultations to improve mandated representation in Family Court appeals in matters such as records, briefs, and oral arguments.
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