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Knowledge of OSHA, FDA, and HIPAA compliance. Current fields of Regenerative Aesthetics, Regenerative Sexual Medicine, and Regenerative Medicine are well established, clinical research facility requirements in place, and a tissue bank license are in place.
Full-timeExpandApply NowActive JobUpdated 4 days ago - UpvoteDownvoteShare Job
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Excellent knowledge of GxP, ICH guidelines, PhRMA code, FDA CFR, ISO clinical research ethics, HIPAA and patient privacy laws, EU Directive and other applicable local regulations. Knowledge of concepts of clinical research and drug development.
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Ensures compliance with all federal, local, FDA, IRB, and HIPAA guidelines and regulations pertaining to the study and patient care. DEPARTMENT ADDENDUM: Research Associate 1 works directly with Physicians, Clinical Research Coordinator, Research Program Administrator, or Research Nurse, or Principal Investigator to coordinate and/or implement the study and may serve as the point of contact for the external sponsors.
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Ensuring research quality by practicing compliance and following the principles of Good Clinical Practice (GCP)/International Harmonization Conference (ICH), Health Insurance Portability and Accountability Act (HIPAA), Federal Drug Administration (FDA) policies and guidelines, and other applicable regulations (state and local.
$37.86 - $50.48 an hourFull-timeExpandUpdated 9 days ago - UpvoteDownvoteShare Job
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Healthcare Compliance – knowledge of Anti-Kickback laws, false claims act, foreign-corrupt practices act, Physician Payments Act, HIPAA, and FDA regulations. Drafting and negotiating a broad range of agreements commonly needed in the medical device industry, including without limitation supply agreements, clinical trial agreements, research agreements, sales agreements, distribution agreements, consultant agreements.
$90,852 - $136,278 a yearFull-timeExpandApply NowActive JobUpdated 3 months ago - UpvoteDownvoteShare Job
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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.
Full-timeExpandApply NowActive JobUpdated 22 days ago - UpvoteDownvoteShare Job
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Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes.
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Knowledge of HIPAA guidelines; handling Biohazard materials; good clinical practice; FDA and ICH guidelines. Certified Clinical Research Coordinator (SoCRA, ACRP) required within six months of hire date required.
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Essential Job Duties: Ensures the medical well-being and safety of the study participants through the safe performance and ethical execution of the clinical trials, in adherence with FDA, ICH, NIH, GCPs & HIPAA guidelines, study protocols, as well as company policies and processes Overall site leadership with a focus on enhancing efficiencies, patient safety and protocol/GCP /regulatory compliance Evaluates and assesses participants to ensure only eligible participants enroll into the trials.
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11) Observe all health and safety requirements, maintain standards of practice consistent throughout BH, and ensure that the records are in compliance with safety codes set out by regulatory agencies such as the Joint Commission, Department of Public Health (DPH), HIPAA, Food and Drug Administration (FDA), National Fire Protection Association (NFPA), and National Electrical Code (NEC.
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Complete annual reports to Institutional Review Board, CSTA, FDA and other regulatory agencies. The department also engages in cutting edge research, encompassing a wide spectrum of programs in basic, translational, clinical, health services and medical education.
Full-timeExpandApply NowActive JobUpdated 11 days ago - UpvoteDownvoteShare Job
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Experience working in the healthcare industry or a regulated industry (HIPAA compliance, FDA, etc) By advancing how we detect, diagnose, and address cognitive and brain disorders - leveraging cutting-edge neuroscience, clinical expertise, and artificial intelligence - our goal is to enable a future where people can live longer, happier, and healthier lives with better brain health.
ExpandApply NowActive JobUpdated 10 days ago - UpvoteDownvoteShare Job
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Adhere to compliance guidelines throughout processes (OSHA, FDA, HIPAA) Adhere to compliance guidelines throughout processes (OSHA, FDA, HIPAA) Must have BLS, NRP, PALS Certification. The ideal candidate will be responsible for providing care to patients while adhering to compliance standards.
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Our client is looking for a Neurology Principal Investigator who will conduct and coordinate the daily clinical trial activities according to ICH/FDA/GCP guidelines, local regulations, study protocol, and company policies and processes.
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Provide advice in regulatory areas such as, for example, HIPAA, Medicare, Medicaid, Stark law, Anti-Kickback Statute, Affordable Care Act, human subjects research, FDA compliance, ICH Good Clinical Practice, and clinical conflicts of interest.
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