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Clinical Quality Specialist Benefits At TidalHealth, team members working at least 36 hours per pay period based on 12-hour shift schedules or at least 37.5 hours for non 12-hour shift schedules and part-time team members working at least 30 hours or more on weekends only are eligible for benefits.
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Position Information Recruitment/Posting Title Program Development Analyst - Quality Improvement, Assessment, and Accreditation Specialist Job Category Staff & Executive - Project/Program Management/Planning Department RWJ-Education-PISC Overview New Jersey’s academic health center, Rutgers Biomedical and Health Sciences ( RBHS ) takes an integrated approach to educating students, providing clinical care, and conducting research, all with the goal of improving human health.
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Must be willing to travel up to 20% of the time for client work within the US. Requirements: College graduate in scientific, medical, clinical discipline or related experience; or minimum of 7 years’ experience in GCP regulated industry if not a college graduate Minimum of 5 years’ experience in GCP regulated industry (i.e., Clinical Research Coordinator, Clinical Research Associate, or GCP Auditor.
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PROGRAM DESCRIPTION The Frederick National Laboratory is a Federally Funded Research and Development Center (FFRDC) sponsored by the National Cancer Institute (NCI) and operated by Leidos Biomedical Research, Inc. The lab addresses some of the most urgent and intractable problems in the biomedical sciences in cancer and AIDS, drug development and first-in-human clinical trials, applications of nanotechnology in medicine, and rapid response to emerging threats of infectious diseases.
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Minimal travel What we’re looking for in you: Required Qualifications: Bachelor’s degree in Life Sciences, Engineering, or related field Minimum of 7 years of Clinical Quality Systems, Clinical Operations/Project Management, or Regulatory Affairs experience Medical device industry experience required Working knowledge of FDA, ISO, EU MDR, and medical device industry quality requirements governing human subject research.
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The Senior Quality Assurance Specialist - Medical Device has knowledge of regulations and standards governing medical Imaging, AI/machine learning and software as a medical device (SaMD.
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As one of the top five life science companies, we are a global leader in developing, manufacturing, and marketing a broad range of high-quality research and clinical diagnostic products.
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Monitor vendors and clinical investigator sites to ensure processes are followed and quality is maintained independently. Join us at MMS and be part of a team that is shaping the future of clinical research.
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MMS is a award-winning, data-focused clinical research organization (CRO). Expertise within CROs and scientific and clinical data/ terminology, and the drug development process. Hands-on experience with clinical trial and pharmaceutical development preferred.
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Assists in other duties relating to overall compliance within Quality and Compliance department, as requested. Experience in reviewing and editing QMS related documents, i.e., SOPs, Work Practices, Forms, Training Materials, etc.
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The incumbent participates in the implementation and maintenance of the quality management system (QMS), with a focus on one or more program areas, including collection of blood and cellular therapy products, manufacturing and distribution, clinical services, transfusion services, laboratory services, and clinical research, as well as organization-wide support functions such as information systems, facilities, and safety.
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Minimum of 5 years’ experience in GCP regulated industry (i.e., Clinical Research Coordinator, Clinical Research Associate, or GCP Auditor.) College graduate in scientific, medical, clinical discipline or related experience; or minimum of 7 years’ experience in GCP regulated industry if not a college graduate.
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Quality Specialist II= Bachelor's degree in life sciences, pharmaceutical, biotech or biologics manufacturing, or quality management. Quality Specialist I= Associate Degree in life sciences, pharmaceutical, biotech or biologics manufacturing, or quality management may be considered with strong relevant experience.
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Our client, a global medical device company, has engaged GForce Life Sciences to provide a Clinical Quality Specialist (GCP). Clinical Quality Specialist, GCP, Medical Device/Pharmaceuticals.
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Our client, a US Fortune 250 company and a global medical technology corporation serving customers in Clinical Labs, Health care research & Pharmaceutical industry, seeks an accomplished Quality Inspection Specialist – 3rd Shift.
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clinical research quality specialist jobs Title: quality specialist in Marion, Indiana
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