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May be Principal Investigator and/or Study Director for one or more phases of studies and assist in other phases. In addition to performing as a lead analyst, you will serve as PI on a limited number of Bioanalytical studies and will be responsible for study management, interpretation and reporting of study data, and in concert with Research Scientists and peers, will participate in method validation when needed.
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As TMF Study Owner you will ensure that the clinical trial documentation must be consistent with the Trial Master File (TMF) specifications, submission/inspection readiness criteria and comply with applicable SOPs and other requirements.
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The Assistant Study Coordinator will work to ensure the delivery of quality research and patient safety by adhering to regulatory compliance standards, as dictated by federal regulations, Good Clinical Practice, and local and institutional policies related to the mission of the UNC / LCCC Clinical Trials Office, safeguarding institutional integrity.
$47,660 - $56,000 a yearPart-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Monitors and reports study changes to Study Director and all appropriate personnel. Follows SOPs and Protocols to perform procedures on study and stock animals, including, but not limited to: clinical observations, food consumptions, body weights, urine collection, administering injectable anesthesia, mating procedures, blood draws (all routes), euthanasia/necropsy, catheter placement, restraint, enrichment, and feeding and food removal.
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The Director will be supported a robust clinical trials infrastructure including study start-up, regulatory, contract and budgeting, data management, research nursing, pharmacy, and quality.
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Performs all delegated functions as defined by facility CLIA Director. Performs statistical study (CV, DS, trend study, etc.) Cert Histocompatibility Techno (CHT-ABHI), Clinical Laboratory Scientist (CLS), Medical Laboratory Scientist (MLS), Medical Technologist (MT), Specialist in Cytology-ASCP (SCT), Specialist in Cytometry-ASCP (SCYM), Molecular Biology Spec-ASCP (SMB.
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When required by the Deputy Director represent the OEA by attending legislative committee meetings or other meetings with other organizations. Assist in the preparation and presentation of the OEA Annual Report including preparation of summary of prior year reports, current study topics, and other information as needed.
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Our research programs encompass a broad range of biomedical research activities and areas of study, focusing on various fields such as cardiovascular disease, alcoholism, hematopoietic cancer, behavioral research, aging, and gene therapy.
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Our research aims to improve quality of life, well-being, symptom and pain management, and reduce caregiver burden:For example, a Clinical Research Coordinator to support a large multi-site clinical trial study that focuses on the comparison of care delivery models to support older adults with complex healthcare needs.
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130959 Study Coordinator- Hybrid. Essential job functions include working with PIs to archive websites; developing annotation codebooks; work lead and train coders; processing data per specifications for analysis and storage; recruiting residential households to receive delivers and coordinating with study collect delivers; attending regular study meetings with study staff and investigators and participating in report preparation.
$28.88 - $46.46 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The School Psychologist will work consistently and creatively to meet the needs of all students, be responsible for academic advising and student socialization, collaborate on the Child Study Team, and partner with School Leaders and campus-based Special Education teams to provide related professional development to teachers and staff.
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Utilize CADD skills as trained and required to complete work assigned by Job Captain/Project Manager/Project Director. Adhere to daily schedules and directions from Job Captain/Project Manager/Project Director relative to assigned work/tasks.
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The Director, Clinical Data Management will contribute to the development, planning and execution of clinical studies and will ensure scientific integrity and interpretation of study data of the clinical program(s.
$209,000 - $242,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Reviews study with principal investigator and/or clinical research coordinator to a budget outlining standard of care and research costs. In collaboration with the principal investigator, clinical research coordinator, and clinical team, participates in the review of studies for feasibility and evaluates potential competition with other protocols prior to submitting study.
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The Director of Development will secure philanthropic support and strategic direction for a comprehensive and coordinated development program that includes all aspects of fundraising, including annual fund, corporate and foundation relations, planned giving, and major and principal gifts.
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study director jobs Title: associate research Company: Actalent in IN, Pennsylvania
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