In this role, you will be responsible for implementation of clinical research protocols under physician investigator guidance and delegation and clinical research specialist and/or clinical research coordinator II guidance.
In this role, the selected candidate serves as a liaison for collaborating institutions, human subjects review boards, and commercial partners; provides guidance or assistance on participant screening, consent, data collection and storage.
The Coordinator, Research & Prospect Management will work in the Research & Prospect Management office under the direction of the Director of Research & Prospect Management and will have the primary responsibility of identifying prospective donors and collecting, evaluating, analyzing, organizing, packaging, and disseminating detailed prospect research on current and potential prospects for the Office of Development and Alumni Relations.
In this role, you will direct and oversee Clinical Development/Operations and Regulatory Affairs process for a research and development services provider conducting clinical trials of experimental vaccines and biologics.
The candidate must have on-site clinical monitoring experience including source data verification using medical charts, review of regulatory study binders, adverse events and data clarification process.
S/he is responsible for coordinating and assuring integrity of all activities associated with conducting a clinical trial that involves multiple DoD and VA sites. S/he will ensure compliance with all local, state, federal, and international regulatory requirements.
In this role, you will assist clients with the technical and programmatic management of a portfolio of research and development (R&D) efforts. Serve as a coordinator responsible for managing technical scope, budget, and schedule of multiple projects.
In this role, you will be responsible for
provides assurance of accurate documentation in compliance with all governing regulations.Develop databases or modify existing databases to create datasets for analysis.
In this role, the selected candidate will support the goals of the Gen Med organization by initiating, monitoring, and closing out clinical study sites following GCP and ICH guidelines as well as Novartis SOPs and ensuring that study milestones are met.
In this role, you will provide direction and support to unit staff. Supervises admissions, conducts assessment of patient's needs, and initiates nursing care plans. Evaluates and documents patient progress.
In this role, the selected candidate will coordinate financial aspects of study implementation and management from protocol feasibility through study close-out per company Research Center and Research Department policies and guidelines.
In this role, the selected candidate will oversee professional nursing care and coordination of services provided in various licensed acute hospitals and sub-acute facilities that have contracted with Company to provide dialysis and other services to patients of and under the license of the acute facility.
In this role, you will assist the principal investigator and/or program manager in defining information and plans required to accomplish goals of studies. May help design and create protocol specific data collection forms with assistance.