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As one of the campuses of the University of North Carolina (UNC) system, North Carolina Central University(NCCU) is located in Durham near Research Triangle Park. The Department of CSD is a full-time, campus-based graduate program and features a curriculum that integrates research, evidence-based clinical experiences, and a focus on serving diverse populations.
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Completion of an allied health degree (e.g., Respiratory Therapy, clinical training as a Registered Nurse (RN), Physician's Assistant (PA) or Pharmacist plus four years of healthcare experience; orone of the following equivalents: Radiologic Technology, Licensed Practical Nurse) or Associates degree in Clinical Trials Research related curriculum plus a minimum of six years healthcare experience; or 2.
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Avert crisis situations by assisting the family in times of urgent need (e.g., risk of harm to child or caregiver, pending child removal), in consultation with the Family Resource Partner and Clinical Director.
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Experience as a traveling Clinical Research Associate / Clinical Site Monitor. Previous technical and managerial experience in conducting multi-national and/or local clinical trials in a hospital setting, biotechnology / pharmaceutical company, or CRO; at least two years must have been spent actively managing the full scope of clinical research projects (i.e., accountability across all functional areas including budget ownership.
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RSI employs more than 250 clinical, direct care, nursing, and administrative staff. RSI ranks highly in Orange County, NC: 5th largest non-profit & 15th largest employer RSI's Spring Glen Retirement Community, est.
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Experience Requirements: No Experience Required Clinical - Radiology Required - And 1 Year Clinical - Urgent Care Preferred Select Education Type: Graduate Radiologic Technology Required Licensure/Certification Requirements: Registered Technologist for Radiography Required Hours of Work: Every Other Friday, Saturday, Sunday, Monday Weekend Requirements: Every Other Call Requirements: none.
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The selected candidate will support the in vivo histology analysis of projects within the Preclinical Development team.
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About the role:The Laboratory Technician, Pre-Clinical Vector Manufacturing reporting to the Vector Manufacturing Team Lead is responsible for supporting routine laboratory operations related to manufacturing research-grade recombinant Adeno-associated virus (rAAV) vectors as part ofVector Core. The rAAV vectors manufactured support capsid technology development, intellectual property portfolio and progression of internal and external early-stage gene therapy programs.
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Hands on experience with bioanalytical method development, validation, and sample analysis for the extraction and quantitation of specific nucleic acids for CMC, preclinical and clinical studies.
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Out client is seeking a dedicated and experienced Clinical Research Associate (CRA) to join their team on a full-time basis. About the job Clinical Research Associate (Hybrid) Basic knowledge and application of clinical research regulatory requirements, including GCP and ICH guidelines.
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The CAS support BioFire (BFDX) customers, distribution partners, BioMerieux (BMX) subsidiaries/distributors, BMX Global Customer Support, and the BFDX Sales network (Sales Managers, Clinical Implementation Managers, Corporate Account Managers, Field Applications Specialists, etc.
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Develop, qualify, and validate (as appropriate) bioanalytical assays (expressions assays including mRNA and protein [ELISA/IHC], anti-AAV capsid nAb, CTL IFN-γ ELISPOT, IgG/IgM, biodistribution and shedding) for all programs and define science-driven, phase appropriate, and risk-based analytical development strategies to support the development candidate during discovery through preclinical evaluation (including GLP) and clinical development advancement.
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To be responsible for Epidemiological studies within a large program or group of related programs (led by a senior epidemiologist) within the context of the GSK Vaccines process in order to ensure the high quality and on-time delivery of all epi data that will allow and support world-wide registration in compliance with the clinical and epi development plan, applicable good practices, and GSK Vaccines standard operating procedures (SOP.
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Marken offers a state-of-the-art GMP-compliant depot network and logistic hubs for clinical drug product storage and distribution worldwide, and supports cell and gene therapy logistics services from clinical to commercial, while maintaining the leading position for Direct-to-Patient and Home Healthcare services, biological sample shipments and biological kit production.
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Certified Clinical Hemodialysis Certification (CCHT) certification. Initiates renal replacement treatment according to prescribed orders including setting blood flow rate (QB) and dialysate flow rate (QD) or peritoneal dialysis as prescribed by the attending nephrologist.
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hrsa clinical jobs in Durham, NC
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