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Provide technical support for the implementation of REACH activities in buy-in countries, with a focus on improving the quality of clinical and community case management, strengthening referral systems, and pre- and in-service capacity building in case management, MiP, and SMC.Support the development of and review of annual reports, tools and guidance, and other relevant deliverables, ensuring high-quality documents and deliverables.
ExpandApply NowActive JobUpdated 8 days ago - UpvoteDownvoteShare Job
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Experienced in coordinating project meetings, electronic medical records, protocol review revision, patient confidentiality, remote site monitoring, regulatory compliance, protocol development, clinical research, clinical trials, and protocol writing.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Serve as the Scientific Review Chair in the development of VRC clinical trial protocols to provide subject matter expertise and scientific oversight. Our core practice areas include: clinical research; vaccine research, microbiology and infectious disease research, development and production; biodefense; global health security; and HIV/AIDS programs.
$67,000 - $90,000 a yearFull-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Our PICU RN will use clinical expertise for the review of medical records against appropriate criteria in conjunction with contract requirements, critical thinking, and decision-making skills to determine if the Standard of care was met during the episode of care in question, while maintaining production goals and QA standards.
RemoteExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Develop and manage detailed project schedules and work plans for CIVICs vaccine manufacturing, toxicology, clinical testing, and related projects and activities. Coordinate the review of preclinical vaccine data packages with duties including organizing review meetings with NIAID staff and the CIVICs Steering Committee, collating feedback, and ensuring that review timelines are met.
Full-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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Additional Required Licenses/Certifications/Posting Specific Minimum Qualifications: Diplomat of the American Board of Applied Toxicology (ABAT), OR7 years of experience as a CSPI with a minimum CSPI exam score of 115 points and ABAT-eligibility as determined by ABAT approval to sit for an upcoming ABAT exam or an informal ABAT credentialing review showing the individual is close to eligibility.
Full-timeExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Facilitate the preparation of Institutional Review Board applications for clinical research proposals, develop and manage budgets and coordinates grant applications, progress reports and regulatory documentations submissions as required by the sponsor.
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Assures site research quality by practicing in compliance with US Oncology Research, Inc. (USOR) Standard Operating Procedures (SOP), principles of Good Clinical Practice (GCP) and applicable federal, state, and local regulations through OSHA, CDC and HIPPA. Supports and adheres to US Oncology Compliance Program, to include the Code of Ethics Business Standards.
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The Registered Respiratory Therapist possess sufficient training and experience to perform independent professional respiratory care diagnostic and therapeutic procedures, clinical evaluation of care including the establishment of therapeutic objectives and the review of care.
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The Quality Assurance Nurse (QARN) is responsible for assisting in the development, implementation and evaluation of quality assurance, performance improvement, and utilization review activities as requested by the VP of Organizational Performance/Chief Compliance Officer and the Director of Clinical Performance.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Develops and oversees peer review systems for clinical staff, and coordinates the performance appraisal of the primary care physician. Ensures compliance with PACE provider regulations as they pertain to medical/clinical components of care.
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Enters data into the clinical software system related to pre-authorization requests for pharmacy, non-pharmacy, case management and hospitalizations. As the medical education and clinical partner of Georgetown University for more than 20 years, MedStar Health is dedicated not only to teaching the next generation of doctors, but also to the continuing education, professional development, and personal fulfillment of our whole team.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Chart Review with aim to promote evidence based medical practice and adherence to D ispatchHealth clinical pathways. Work as part of a clinical care team with a DHMT (Medical Technician) and individually, as appropriate for the service line to deliver care in the patient’s home through our innovative in-home care service lines (i.e., Acute Care, Bridge Care, Advanced Care , Tele-presentation and others.
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Assist with clinical study activities such as study start up, investigator meetings, data review, etc. Work on special projects on the clinical team, such as use of medical review tools and creating and maintaining trackers related to selected safety and recruitment topics.
InternExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Assist Clinical Scientist, Study Responsible Scientist (SRS), &/or Study Responsible Physician (SRP) in various clinical research assigned Immunology Development clinical trials. Clinical Scientist Intern will support the Late Development Immunology team and will support further business, operational and clinical excellence in Immunology.
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