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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.
TemporaryExpandApply NowActive JobUpdated 21 days ago - UpvoteDownvoteShare Job
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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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Works effectively with Development Innovations, Site Management Organization, Corporate Quality, Research Directors, clinical trial Sponsors, clinical study teams, site colleagues, outside consultants, Information Technology Group (ITG), other Sarah Cannon functional groups, and vendors, as needed.
Full-timeRemoteExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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The Andelyn Corporate Center (ACC) is dedicated to cGMP manufacturing, the Andelyn Development Center (ADC) for preclinical non-cGMP activities, and the Andelyn Plasmid Center (APC) for research and cGMP plasmid production.
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Complementing our broad research and development capabilities, Nkarta has also built an extensive cell therapy manufacturing operation. Act as the Quality Lead between Nkarta and Nkarta’s Contract Manufacturing Organizations (CMO) sites for packaging and labelling of clinical drug product.
Full-timeExpandApply NowActive JobUpdated 17 days ago - UpvoteDownvoteShare Job
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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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Join us at MMS and be part of a team that is shaping the future of clinical research. Monitor vendors and clinical investigator sites to ensure processes are followed and quality is maintained independently.
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Minimum of 5 years’ experience inGCP regulated industry (i.e., Clinical Research Coordinator, Clinical Research Associate, or GCP Auditor.) MMS is aaward-winning, data-focused clinical research organization (CRO.
Full-timeExpandApply NowActive JobUpdated 18 days ago - UpvoteDownvoteShare Job
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Assists in other duties relating to overall compliance within Quality and Compliance department, as requested. 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.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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Assists in evaluation, analysis, maintenance and development of system functionality of the EHR to meet clinical objectives including participating in project plan development/tracking and workflow analysis.
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Experience in reviewing and editing QMS related documents, i.e., SOPs, Work Practices, Forms, Training Materials, etc. We support the pharmaceutical, biotech, and medical device industries with our proven, scientific approach to complex trial data and regulatory submission challenges.
Full-timeExpandApply NowActive JobUpdated 25 days ago - UpvoteDownvoteShare Job
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With a global footprint across four continents, MMS not only maintains an industry-leading customer satisfaction rating but also fosters a collaborative and inclusive work environment where employees can thrive.
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Discover more about our exciting opportunities and why MMS is a great place to advance your career. Proficient with 21 CFR Part 11, FDA, and GxP requirements. We pride ourselves on being a Great Place to Work certified organization, recognized for our exceptional culture and industry best employee retention rate.
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Maintains a strong understanding of regulations and guidance as they pertain to compliance; maintains knowledge relating to regulatory updates. Are you looking to join a company where your contributions truly matter, and where you'll be part of a supportive, innovative team.
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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 graduateMinimum of 5 years experience in GCP regulated industry (i.e., Clinical Research Coordinator, Clinical Research Associate, or GCP Auditor.
Full-timeExpandApply NowActive JobUpdated 25 days ago
clinical research and development jobs Title: quality specialist in Marion, Indiana
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