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The Quality Vendor Manager, is responsible for managing the qualification of vendors providing services related to clinical trials and Bioanalytical services, ensuring compliance with Good Clinical Practices (GCP) and Good Laboratory Practices (GLP) regulations and quality standards.
$95,000 - $135,000 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are looking for a highly motivated, positive and innovative senior level Clinical Research Study Coordinator (Research Coordinator) to lead in the coordination, management and conduct of nephrology clinical research trials in dialysis centers and physicians practices.
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Oversight of equipment quality assurance and development of clinical tools for diagnostic (breast, cardiac, pancreas), therapeutic (interventional radiology, radiation oncology image guidance), and follow-up clinic (rehabilitation, treatment late effects) applications.
$72,071 - $93,730 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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This individual will be responsible for conducting hatchery quality assurance assessments including fertility, hatchability and chick quality evaluations. Hatchery quality assurance reports will be produced using Excel spreadsheets, MTech, SAP and distributed through the E-Mail system.
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Communication Internal: At Management (e.g., Team Manager, Study Manager) and lower (e.g., QC Auditor, Clinical QC Reviewer) levels with the following departments: QA, clinic, bioanalytical, PK, Biostatistics, IT, TSS.
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Basic computer literacy Strong written and verbal communication skills Experience in quality assurance, food safety management systems, meat, and poultry HACCP and SQF Practitioner certification is desired.
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Performs work independently, under the general guidance of the supervisor and is responsible for providing Quality Assurance (QA) and quality control oversight of clinical trials, to include coordinating Good Clinical Practice (GCP) monitoring of non-Investigational New Drug (IND) and IND protocols domestically and internationally; general QA for data; and the development and maintenance of databases tracking essential study documents and data for reports.
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As a Failure Analysis Engineer, the candidate will be reporting to the Director of Quality Assurance and will be interacting with internal customers and key support groups (Customer Quality, Product/Test Engineering, Design, Applications Eng., Packaging Eng. and others.
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The Clinical Trials Monitor helps to ensure compliance of the clinical research enterprise with all related regulatory policies and guidelines, including federal, state, local, as well as the policies and procedures outlined by the Dana-Farber Cancer Institute and Dana-Farber Harvard Cancer Center (DF/HCC) consortium.
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The Clinical Quality Assurance RN will review for to confirm accuracy and monitor timeliness in accordance with the Fidelis Care’s policies and regulatory standards, ensuring adherence to departmental and regulatory data integrity standards and requirements including contractual obligations with State and Federal agencies such as New York State Department of Health (NYDOH), County Department of Health (CDOH), Local Department of Social Services and Center for Medicare & Medicaid Services (CMS.
$67,400 - $121,300 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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We are looking for a Quality Assurance (QA) Specialist. The QA Specialist will also support the production team with other quality initiatives as needed. Other duties and projects as assigned by the Quality Manager.
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Creates, completes and compiles necessary documentation related to Quality Inspection as per OEM and ISO/AS standards. Minimum of 7 years related quality inspection experience. The primary purpose of this job is to support the Quality Manager System and perform 1st piece, in-process, final, and source inspections as required by work instructions.
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The Quality Assurance Manager is responsible for overseeing and ensuring the highest standards of quality and safety in the production of Pepperidge Farm branded Cookies and Crackers, including iconic brands such as Milano cookies and Goldfish crackers.
$85,900 - $140,800 a yearFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Clinical Trials Office (CTO) at UCSD's Moores Cancer Center administers many clinical trials on behalf of its member investigators, including trials sponsored by National Cancer Institute cooperative groups, pharmaceutical companies, and physician investigators.
$34.78 - $57.6 an hourFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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The Associate Director, Quality Systems and Compliance is responsible for developing strategy and managing activities involving GMP Quality Assurance and compliance with applicable regulatory requirements, development and implementation of Quality Assurance policies and procedures, and to ensure quality standards in compliance with relevant regulatory and quality guidelines for Good Manufacturing Practices.
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clinical trials quality assurance jobs Title: clinical director Company: Virginia Commonwealth University in Chalmette, Louisiana
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