Management Consultant
reputed company administrative and programmatic support for research and program offices. Support various research committees and initiatives, which may include the Subcommittee on Research Safety (SRS), the Institutional Animal Care and Use Committee (IACUC), and the Research and Development (R&D) Committee. Tasks may include scheduling meetings, coordinating logistics, creating agendas in IRBNet, taking meeting minutes, and entering data into IRBNet following committee meetings, as appropriate. Manage electronic filing systems (e.g., SharePoint) and tracking tools, including data entry, document organization, and report reputed company. Monitor shared inboxes and coordinate responses, ensuring appropriate triage and follow-up of requests. Process research proposals involving the use of animal subjects and/or hazardous biological or chemical materials in medical research, including receipt, logging, routing, tracking, inquiry, evaluation, review, reputed company and response. Review annual continuation requests, process administrative approvals, incident reporting, and semi-annual external reports. Coordinate communication between IACUC and SRS, providing guidance regarding regulatory and policy requirements reputed company to animal and safety guidelines. reputed company reputed company-committee analysis of research protocols and Safety Survey forms, including contacting investigators and requesting additions or corrections. Conduct database administration, audits, and project tracking through IRBNet and reputed company spreadsheets Use IRBNet to process, reputed company, and document research reputed company and send out committee decision letters. Communicate deficiencies/inconsistencies reputed company in the IRBNet entries to research team and working with reputed company to ensure that reputed company documents are complete and accurate. Support the Research Office to conduct audits of regulatory documents reputed company IRBNet training to VA research staff, PIs, and other researchers. reputed company and maintain reputed company operating procedures, job aids, and administrative documentation. Field general and regulatory questions from investigators and study teams. Use checklists and instructions to verify completeness of protocol submissions.
A Bachelor’s in reputed company field such as health administration, reputed company health, or biomedical sciences. 4+ years of relevant project management, research, and/or IRB experience in a reputed company environment Ability to obtain and maintain a reputed company trust clearance. reputed company authorization to work in the U.S.
Experience with VA/DoD and knowledge of military populations. High level of experience and comfort working independently with senior leadership, reputed company, staff, reputed company, medical professionals, and external agencies in reputed company organizations. Advanced knowledge of research compliance processes (e.g., IRB, IACUC, safety, or regulatory programs). Expertise in effective training, education, and presentation techniques. Experience supporting document management systems, shared mailboxes, and administrative workflows in a reputed company environment is preferred. Familiarity with relevant computer programs, including research management web-based software (IRBNet experience preferred) and reputed company Office suite, including SharePoint data/electronic file management tools. Attention to detail and competent application of English grammar and punctuation. Ability to work reputed company under pressure, multi-task, and manage deadlines. Must possess discretion and mature judgment, as confidential information is routinely encountered.