- HonorHealth (AZ)
- …review requests, protocol deviations, and information required from the Principal Investigator . Audits compliance of policies and documentation requirements for the ... Health and Human Services (DHHS) regulations: 45 CFR 46, and Food and Drug Administration (FDA) regulations: Title 21 Code of Federal Regulations. This includes… more
- Teleflex (Minneapolis, MN)
- …visit report. o Works collaboratively with Research Coordinators and Investigators to conduct monitoring visits, provide retraining, and resolve compliance ... team, department, and study-related projects as requested, including audits, investigator meetings, training, etc. o Interfaces with Clinical, Regulatory, Sales,… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …a resource to the Emory research community and healthcare professionals and to investigators in the development of investigator -initiated studies. + Oversees the ... and dispenses investigational drugs and materials issued by the Investigational Drug Service for ongoing research studies. + Manages required record-keeping,… more
- Muckleshoot Indian Tribe (Auburn, WA)
- …assignment to the position. + Conduct face-to=face interviews with investigator , children, parents, caregivers, alleged perpetrators and/or all other official ... necessary. + Attend mandatory and/or approved training. + Work collaboratively with investigators . + Work with Tribal youth to build critical awareness around the… more
- University of Colorado (Aurora, CO)
- …to ensure compliance with requirements of the Food and Drug Administration (FDA), study protocols, department, hospital/clinical standard operating procedures ... is seeking a Research Nurse to assist with both industry and investigator -initiated clinical research protocols. The research nurse will work closely with and… more
- Georgetown Univerisity (Washington, DC)
- …bowel) and GI clinical research studies, under the oversight of the Principal Investigator (PI) and direct supervision of the Clinical Trials Supervisor as well as ... and conducts the studies under direct oversight of the Principal Investigators (PIs). This individual will interact directly with patients, research participants,… more
- AbbVie (Irvine, CA)
- …of the overall Product Development Plan. + Oversees project-related education of investigators , study site personnel and AbbVie study staff. + Responsible for ... the clinical studies, clinician reported outcomes, patient reported outcomes and global drug development. Specifically in the area of aesthetic toxin development. +… more
- Veterans Affairs, Veterans Health Administration (Washington, DC)
- …approved data management systems. Collaborates with the site Principal Investigator (Physician) and study co- investigators , Pathology, Interventional Radiology ... in a testing designated position are subject to urinalysis to screen for illegal drug use prior to appointment. Applicants who refuse to be tested will be denied… more
- Grifols Shared Services North America, Inc (Indianapolis, IN)
- …meet their needs + Serves as a conduit for research for investigators interested in developing investigator -initiated research protocols + Strengthens alliances ... representing Grifols' position and interests regarding research, current and future drug development and corporate mission + Adheres to company policies and… more
- University of Virginia (Charlottesville, VA)
- …to apply (examples include, but are not limited to: vaccine, drug , therapeutic, and device development, bioengineering, biomanufacturing)._** All research fields ... (AAHRPP) and as such can act as the IRB of record for multi-site investigator initiated trials; the UVA IRB also accepts National Cancer Institute (NCI) Central… more