- University of Miami (Miami, FL)
- …procedures according to the protocol. + Coordinate routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. + Address adverse events per protocol, advocating for study … more
- University of Miami (Miami, FL)
- …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. + Addresses adverse events per protocol, advocating for study … more
- Cedars-Sinai (Los Angeles, CA)
- …information; present this information at regular research staff meetings. + Notifies direct supervisor about concerns regarding data quality and study conduct. + ... Children's. The Clinical Research Coordinator I works independently providing study coordination, screening of potential patients for protocol eligibility,… more
- HCA Healthcare (Savannah, GA)
- …with reconciling study payments at the site . Actively engage in tracking of studies conducted at the site . Oversee study progress at the site from initial ... proposed budgets for adequate coverage and recommends changes to Supervisor . Facilitate contracting with hospitals, provider groups, and/or...submission of feasibility until study closeout . Coordinate submission and approval for the… more
- Veterans Affairs, Veterans Health Administration (Dallas, TX)
- …effectiveness and/or productivity. Performs organizational and/or staffing utilization studies . Identifies and develops staffing and-work- methods efficiency ... improvement plans. Plans, develops and conducts internal review studies . Develops proposals to restructure program areas that require redistribution of significant… more
- Veterans Affairs, Veterans Health Administration (Iowa City, IA)
- …sleep latency recordings, intraoperative monitoring, evoked potentials, home sleep studies and nerve conduction studies . Responsibilities This announcement ... testing ( EEG, NCV, Evoke Potential or Home sleep study ). Prepare and calibrate equipment required for testing to...with the assistance of the Lead Tech or Lab Supervisor Follow procedural protocols for all END testing to… more
- University of Rochester (Rochester, NY)
- …**Responsibilities:** Responsible for setting up IR rooms specific to the study being conducted. Utilizes customer service skills while interacting with patients ... on various shifts. Leads may either assist their shift supervisor , or in the absence of a supervisor...Responsible for setting up IR rooms specific to the study being conducted. Utilizes customer service skills while interacting… more
- University of Pennsylvania (Philadelphia, PA)
- …will directly oversee, train and mentor any reporting Regulatory Affairs Supervisor and/or Regulatory Affairs Specialist A/B/C. In this capacity, the Associate ... applicable regulatory bodies. In conjunction with any reporting Regulatory Affairs Supervisor , the Associate Director for Regulatory Affairs will evaluate regulatory… more
- The County of Los Angeles (Los Angeles, CA)
- …allocable to this class typically report to a higher-level clinical supervisor and independently provide the full range of professional psychological services ... of cases, including identifying treatment outcomes. + Obtains and studies medical, psychological, social, and family histories by interviewing individuals,… more
- University of Utah (Salt Lake City, UT)
- …trial activities in compliance with Good Clinical Practice ( GCP ), study protocols, and applicable IRB regulations. Implement and manage processes to support ... study objectives, including development and maintenance of IRB protocols,...with some hybrid options available with prior consultation with supervisor . **Learn more about the great benefits of working… more
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