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the Principal Investigator with study development, grant submissions, study execution, data management, quality control, regulatory activities, reporting, and the preparation of reports and manuscripts, while
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background. Consideration to interview will also be given to applicants who are in the process of completing the required PhD, MD, or PhD/MD degree. Documentation of the required PhD, MD, or PhD/MD degree
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programs (Word, Excel, PowerPoint, etc.) for report writing, data graphing, recordkeeping, website update, and inventory control is required. Ability to quickly learn new techniques and instrumentations
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, R, Mplus, or similar; skills in PROCESS, SEM (and CFA)—specifically multigroup modeling and invariance testing. Writing proficiency. IRB protocol and submission process Preferred Qualifications PhD in
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Date 09/25/2026 Qualifications Minimum Education and Experience Co-Adjutant faculty are expected to have graduated from a Masters or PhD program in Public Administration or an affiliated field
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Research Associate also assists the Principal Investigator with study development, grant submissions, study execution, data management, quality control, regulatory activities, reporting, and the preparation
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providing clinical care to all animals, experimental surgery, and surgical and anesthesia support. Supports or serves as the Registration Coordinator for the Controlled Dangerous Substances Program. FLSA
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control, and research integrity, while supervising a team of program professionals. Ensures institutional compliance with federal, state, and university regulations, including but not limited to NSPM-33
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Qualified candidates are required to have a PhD or an equivalent doctoral degree and experience in chemistry, biology, toxicology, pharmaceutical science, computer science, or statistics. Candidates must have
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. Successful candidates may come from any relevant discipline. All requirements for the PhD or other terminal degree in the relevant field must be completed by August 1, 2027. A record of publication and