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Collaborate with NIH clinical research scientists, Principal Investigators, Research Coordinators, Protocol Navigators, NINDS Sponsor representatives, CTU staff, and safety, regulatory, and monitoring entities.
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For the scientific advancement of clinical research, CMRPD services include comprehensive clinical trials monitoring, regulatory, pharmacovigilance, protocol navigation and development, and programmatic and project management support for facilitating the conduct of 400+ Phase I, II, and III domestic and international trials on a yearly basis.
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Provide telecommunications support to include but not limited to: system order construction and validation (circuits, wireless, satellite), programming and configuration Private Branch Exchange (PBX), Voice over Internet Protocol (VoIP), Secure Terminal Equipment (STE), wireless, voicemail, system deployment (desktop, wireless, circuits), and infrastructure maintenance and deployment (copper, fiber, peripheral equipment.
$36.7 an hourFull-timeExpandApply NowActive JobUpdated Yesterday - UpvoteDownvoteShare Job
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Experience with Department Information Systems Agency (DISA) Security Technical Implementation Guidelines (STIGs) / Security Requirements Guide (SRG), applicable to each non-classified or Secret Internet Protocol (IP) Router Network (NIPRNet, SIPRNet) environment for all ESS implementations.
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He/she will provide timely and accurate guidance to investigators on the preparation and submission of new or renewal IACUC protocol applications, protocol amendments/revisions, and related documents.
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Responsibilities: Conducting all trial visits Completing all study-specific assessments (e.g. vital signs, EKG, blood collection) Processing all samples and shipping to Central Lab Maintaining study source Entering data into sponsor EDC and query resolution as the sole Senior Clinical Research Coordinator (SCRC) on-site, the chosen candidate must be adept at protocol comprehension and be capable of working autonomously.
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In this role the Research Nurse Coordinator screens, enrolls, plans, implements, and evaluates protocol-related care of participants and data for assigned research projects. Follows study-specific protocol guidelines, communicates, and interacts with investigators, hospital staff, department manager, sponsoring agencies, and others to effectively perform clinical research activities.
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CTA chest, neck, abdomen Occasional CTA Cardiac studies Some CT Lumbar / Thoracic spine CT Head Stroke protocol Best personality Fit: · Works well in a department that could be busy or slow based on the ED patient load.
$2,203.82 - $2,539.19 a weekFull-timeExpandApply NowActive JobUpdated Today - UpvoteDownvoteShare Job
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Christiana Care Health System is currently seeking a Research Nurse Coordinator with two years of Oncology Clinical experience for our Cancer Research Department at the Helen F. Graham Center & Research Institute in Newark, DE.
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In addition to acting as a clinical research coordinator, the RN is also responsible for drug administration, phlebotomy and pharmacokinetic sampling, toxicity checks, and protocol specific tests and procedures specifically related to clinical research studies as well as other clinical duties such as EKGs and Holter monitors as assigned based on appropriate licensure and/or completion of competency documentation and team needs.
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Knowledge of how traffic flows across the network (e.g., Transmission Control Protocol [TCP] and Internet Protocol [IP], Open System Interconnection Model [OSI], Information Technology Infrastructure Library, current version [ITIL.
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Collect, analyze and integrate patient information in order to identify and meet the patient-specific needs and determine final testing parameters/protocol in conjunction with the ordering physician or clinical director and the sleep lab protocols.
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Responsibilities of the Medical Technologist (MT) (MLT) (MLS) (CLS)Abide by laboratory protocol and procedures. Please note - our client does NOT offer H1b visa sponsorship. Requirements of the Medical Technologist (MT) (MLT) (MLS) (CLS)ASCP or equivalent certification requiredAS/BS Degree in Medical Technology or related science requiredComfortable working in all areas of the lab.
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Coordinates all aspects of protocol treatment and monitoring and ensures everything is completed and documented. Creates methods and systems to ensure patient compliance with protocol procedures, uses a problem-solving process when non-compliance occurs.
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Instruct patient and family members on proper use of equipment such as wheelchairs, braces, walkers, crutches, canes, and other prosthetic/orthotic devices Policies: Completes all clinical documentation following agency protocol and Medicare/Federal guidelines.
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protocol job Title: coordinator clinical trial
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