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We are seeking a Veterinary Clinical Research Nurse to provide staff support for clinical trials including data entry, organizing, maintaining and assuring the accuracy of all study documentation under the direction of the supervisor.
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With minimal supervision: the clinical research coordinator will coordinate Phase I-IV clinical trials and registries for the Pulmonary Vascular Disease Program. The Coordinator B will participate in and coordinate clinical trials and clinical studies in the PVD program.
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The role of the Oncology Research Pre-Post Award Associate is to develop the clinical trial agreements, budgets and coverage analyses for industry-sponsored clinical trials that bring new treatment options to our patients; and complete research billing review in Epic; and facilitate research invoicing for industry-sponsored and federally-funded clinical trials; and work collaboratively with Oncology Research Coordinators and Grants Management colleagues to support accurate billing and invoicing.
Full-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Contribute to assessing and implementing computational, algorithmic, and predictive analytics approaches to address assigned biomedical research questions in areas such as retrospective observational research, emulated clinical trials, clinical decision support and population health surveillance.
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Master’s degree or higher training in clinical trials, population health or outcomes research is preferred. The successful candidate will have patient care responsibilities on the in-patient and out-patient services and will have the opportunity to do research in the existing strong clinical trials, health outcomes research programs in the Division.
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The primary role of the Clinical Research Coordinator A/ B (Regulatory Coordinator) is to assist with regulatory needs and ensure compliance of the Department of Radiation Oncology's portfolio of clinical trials and research studies with University of Pennsylvania, FDA, GCP, and other sponsor, federal, state, and local regulations and guidelines.
$52,661 a yearFull-timeExpandUpdated 1 month ago - UpvoteDownvoteShare Job
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Lead and direct the establishment and operation of Avid’s just-in-time manufacturing of PET radiopharmaceutical investigational medicinal product (IMP) at contract manufacturing organizations (CMO) globally to ensure reliable and sufficient supply to Avid/Lilly clinical trials.
Full-timeExpandUpdated 18 days ago - UpvoteDownvoteShare Job
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Candidates will be expected to teach Gyn Oncology fellows, Ob/Gyn residents and medical students and participate in clinical research including clinical trials. Clinical responsibilities may include out-patient consultations for women with gynecologic cancers as well as in-patient consultation and operative care primarily based at Chester County Hospital.
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The position's role focuses on provision of comprehensive statistical support, specifically related to design and implementation of studies, collection and management of study data, patient safety monitoring, statistical data analysis, and interpretation of statistical data for preclinical studies, clinical trials, retrospective studies, epidemiological, and bioinformatics-related research, and summarization and reporting of study results for professional conferences and publication.
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Runs portions of clinical trials from startup to closeout, including protocol coordination (screening, recruiting, enrolling, consenting), feasibility planning, data management, biological specimen management, preparation for monitoring visits, and regulatory and/or IRB document preparation.
Full-timeExpandApply NowActive JobUpdated 28 days ago - UpvoteDownvoteShare Job
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Partner with key functions (e.g. Clinical Supply, Clinical Development, Clinical Operations, and Clinical Imaging Operations) in the planning and execution of a manufacturing strategy to meet clinical trial supply requirements.
Full-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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Our Clinical Research Division performs all types of Phase II-IV clinical trials in multiple therapeutic areas through a flexible nationwide network of site locations and virtual capabilities.
$90 an hourPart-timeExpandUpdated 18 days ago - UpvoteDownvoteShare Job
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The Clinical Research Coordinator A will also be responsible for training new personnel who will be working on clinical trials within the division. The Clinical Research Coordinator A will recruit and screen patients as outlined in research protocols, will coordinate all research visit activities for assigned projects (including processing and shipping blood and urine samples), and will assist in the maintenance of research records in compliance with IRB and HIPAA regulations.
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Thorough understanding of clinical drug development, GMP, GCP, and familiarity with regulatory (FDA, Health Canada, and other global regulations) requirements for the conduct of clinical trials, including investigator-initiated studies.
ExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Clinical Research Coordinator C:The Clinical Trials Coordinator C will have the same duties as B but will include the following:This individual will work independently with minimal supervision.
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clinical trials jobs in Philadelphia, PA
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