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Reporting to the Clinical Research Manager of Blood & Marrow Transplantation and Cell Therapy (BMT-CT), the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to to manage data, enroll and follow patients on trial, and assist with regulatory and financial requirements of the trials.
ExpandApply NowActive JobUpdated 5 days ago - UpvoteDownvoteShare Job
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Plan, develop, and execute relevant bench-top, pre-clinical and cadaver studies as needed for regulatory, clinical and R&D requirements. About the Role : The Sr. Research and Development Engineer will be helping to advance the company’s minimally invasive low back pain technology, Intracept.
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Medical Strategy: Develop and execute the medical affairs strategy in alignment with corporate goals, ensuring the integration of medical initiatives with clinical development, regulatory affairs, and commercialization efforts.
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NCH is transforming into an Advanced Community Healthcare System(TM) and we’re proud to: Provide higher acuity care and Centers of Excellence; Offer Graduate Medical Education and fellowships; Have endowed chairs; Conduct research and participate in national clinical trials; and partner with other health market leaders, like Hospital for Special Surgery, Encompass, and ProScan.
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Experience with research protocols and regulatory or governing bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices.
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Significant knowledge of clinical study design, outcomes research, and critical review of literature. As a key cross-functional constituent, this employee will work closely with functions across the organization - Marketing, Regulatory Affairs, Clinical Development Engineering (CDE), Global Access Value Economics (GAVE), and commercial functions to ensure scientific accuracy and meet business objectives.
Full-timeExpandApply NowActive JobUpdated 9 days ago - UpvoteDownvoteShare Job
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Reporting to the Clinical Research Manager of Cancer Cell Therapy (CCT), the Clinical Research Coordinator Associate will be conversant in the goals, mission and priorities of the Institute, and utilize this knowledge to to manage data, enroll and follow patients on trial, and assist with regulatory and financial requirements of the trials.
$27.88 - $36.54 an hourFull-timeExpandApply NowActive JobUpdated 1 month ago - UpvoteDownvoteShare Job
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Build, maintain and advance partnerships with key stakeholders across Regulatory Affairs, Clinical Development, PDM, CMC Regulatory, Quality Assurance, Commercial functions, Information Technology and Development Systems to advance near-term regulatory priorities and long-term innovation efforts with broader enterprise level objectives.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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This position works very closely with external vendors, HCPs, as well as multiple Iovance teams: Commercial, Medical Affairs, Regulatory, Safety, Clinical, Biometrics, Quality, Legal, Quality, Supply Chain & Logistics and Manufacturing.
Full-timeExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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Palo Alto Veterans Institute for Research (PAVIR) supports the nation's second largest research program conducted among the VA Hospitals and is looking for a full-time Clinical Research Nurse - TMS. The position is for a nurse practitioner researcher for a VA cooperative clinical study in the division of Psychiatry.
$141,440 - $145,600 a yearFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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This is a full-time on-site role as a Clinical Research Coordinator at CDE medical and LCGK research Clinic located in San Carlos, CA. The Clinical Research Coordinator will be responsible for assisting in the coordination and management of clinical trials, including participant recruitment, screening, enrollment, and follow-up, as well as compliance with study protocols, regulatory standards, and Good Clinical Practice.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Relevant experience includes clinical research and development, regulatory affairs, or related industry/academic experience. You will lead medical writers and collaborate with cross-functional teams (eg, Regulatory, Clinical Development, Patient Safety, and Biometrics) to deliver high-quality documents on time.
ExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Extensive working knowledge of FAR, Cost Accounting Standards, Office of Management and Budget circulars, sponsored guidelines, clinical research regulatory environment, including FDA, regulations, IRB review and approval process and Good Clinical Practice (GCP.
ExpandApply NowActive JobUpdated 3 days ago - UpvoteDownvoteShare Job
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The Clinical Research Operations Specialist II will be responsible for the management of virtual and multisite operations by ensuring adequate study start up, regulatory submissions and training of each of the study sites in preparation for site activation.
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We specialize in developing Samsung’s upcoming software-based medical devices and health services, including product definition and strategy, partner integrations, UI/UX design, usability research, clinical validation, regulatory submissions, and software development/lifecycle.
$172,700 - $237,650 a yearFull-timeExpandUpdated 24 days ago
clinical research regulatory jobs in Palo Alto, CA
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