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You will learn about the scientific, ethical, and organizational underpinnings of clinical research and medicine in general. Working with us as an emergency department (ED) research coop student is a great way to experience medicine and clinical research.
TemporaryExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Medical and Scientific Affairs serves a critical internal leadership and customer-facing support role, including pre- and post-market partnership to functions such as product management, sales and marketing, R&D, Clinical Affairs, Regulatory Affairs, Quality Assurance, Innovation, Strategy, Pharmaceutical Partnerships (Companion Diagnostics), and Technical Support.
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The Research Nurse manages and coordinates all aspects of conducting clinical trials, both clinically and administrative/regulatory. Screens, consents, enrolls and follows study subjects and oversees the same by non-RN clinical research coordinators, ensuring protocol compliance and close monitoring while subjects are on study.
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Regularly interfaces with team members in R&D including Biostatistics and SAS Programming staff, Data Management, clinical research and operations teams, regulatory affairs, clinical pharmacology, medical writing, medical affairs and quality management.
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In addition to TVE, our technology includes a robust AAV manufacturing platform and onsite manufacturing facility that allows us to rapidly produce and test research grade material and scale up to GMP clinical material.
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MINIMUM JOB REQUIREMENTS BA/BS in life sciences or equivalent; or RN/BSN. Advanced degree or certification preferredAt least 6 – 8 years of clinical research experience, with a minimum of 4 years having effectively led a project from inception to completion coupled with demonstrated ability to hold team members accountable with minimal oversight.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Experienced in coordinating project meetings, electronic medical records, protocol review revision, patient confidentiality, remote site monitoring, regulatory compliance, protocol development, clinical research, clinical trials, and protocol writing.
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The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. Prior clinical research or related experience (e.g. monitoring of clinical studies, knowledge of drug development phases, statistical research methodology experience.
Full-timeExpandApply NowActive JobUpdated 6 days ago - UpvoteDownvoteShare Job
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Lead and shape future clinical development strategy and clinical development plans, working closely with Development and Discovery Program Leads and counterparts in Regulatory, Clinical Development, Clinical Operations, Biostatistics, Clinical Pharmacology, Non-clinical and Discovery Research for assigned studies.
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Develop effective collaborations with project leaders and projects team members, including research units, biostatistics, regulatory affairs, clinical pharmacology, human genetics, translational oncology, precision medicine and development operations.
$161,600 - $269,400 a yearFull-timeExpandApply NowActive JobUpdated 7 days ago - UpvoteDownvoteShare Job
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The Senior Research Regulatory Coordinator (RC) works under the direction of the CCI Executive Director, Research Operations Director and Principal Investigator(s) to complete the regulatory requirements of clinical research projects.
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Knowledge of research guidelines and regulatory requirements established by such federal and state agencies as the FDA, National Institutes of Health (NIH), Benaroya Research Institute (BRI) at Virginia Mason and database collection.
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Leads the global Clinical, Pharmacovigilance, and Medical Quality Compliance organization, providing quality oversight of the quality systems supporting Takeda’s clinical research (GCP), pharmacovigilance (GVP) and medical activities across the enterprise and ensuring that it’s robust, aligned with and compliant to applicable regulatory requirements, and governed and positioned for continual improvement.
$205,100 a yearExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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C clinical protocol as approved by the study team and in accordance with all regulatory organizations; manage the regulatory compliance of studies; oversee, supervise, and assist in drafting all reports and other communications required by the NIH or other sponsor The research coordinator should be interested in and capable of developing skills across a number of research methodologies, neuroimaging software, and data analysis tools.
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The Senior Clinical Research Coordinator will develop a progressive functional knowledge of Good Clinical Practices (GCP), Office of Human Research Protections (OHRP) regulations and Food and Drug Administration (FDA) regulations.
ExpandApply NowActive JobUpdated 5 days ago
clinical research regulatory jobs
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