Job Overview:This position provides expert consultation and assistance to faculty, fellow and resident physicians in all aspects of completing a research study. This includes research design and protocol development, grant formulation and writing if applicable, data tabulation, statistical analysis, abstract writing and submission, creation of sophisticated poster presentations, and education regarding the research design and statistical analysis utilized in the study. In addition, this position manages numerous projects and is accountable for ensuring the appropriate steps are being met to keep the project moving in a timely manner. This includes coordination of all necessary paperwork to receive Institutional Review Board (IRB) approval, Institutional Animal Care and Use Committee (IACUC) approval, and research funding. This position works closely with the program director of their specific area and keeps him/her current on all ongoing staff, resident and fellow research projects. This position is required to work with a multidisciplinary team and ensures clear and timely communication throughout the study life.Job Requirements:Master's Degree in a scientific or technical disciplineSignificant and proven clinical research experience including study design and executionStrong aptitude in statistics is required1-2 years experience Professional Clinical Research ExperienceJob Responsibilities:Assists in manuscript writing and editing for publication of research findings in the worldwide medical literature.Completes careful preparation of results, findings and conclusions to maximize likelihood of manuscript publication or acceptance for presentation. Completes careful and professional preparation of slide and poster presentations at national and international medical conferences.Works with multidisciplinary teams to optimize research efforts and to produce quality outcomes by ensuring...Compliance and accuracy in submissions to approval committees. Ensures budget analysis are complete and accurate.Collaborates with clinical staff in developing study documents and processes. Communicates with team members throughout the study process.Develops research protocol designs to ensure implementation and completion of studies within anticipated time frame and budget. Assures that protocols satisfy all federal, state and local requirements while maximizing patient safety, benefit and confidentiality and scientific productivity . Performs literature searches successfully preparatory to protocol writingDesigns, evaluates and validates the appropriate data collection tools to ensure effective data management & documentation, and patient confidentiality. Carefully scrutinizes and audits data to ensure accuracy and completeness.Uses appropriate application and interpretation of parametric and nonparametric statistical analyses including, but not limited to: ANOVA, Linear, logistic and subset regressions, life table analyses, odds-ratio determination, risk factor analysis, study t test, Chi square. Appropriately applies statistics to determine sample size.Other Job-Related Information:Working Conditions:Climbing - RarelyConcentrating - ConsistentlyContinuous Learning - ConsistentlyHearing: Conversation - ConsistentlyInterpersonal Communication - FrequentlyKneeling - OccasionallyLiftingTriHealth is an equal opportunity employer. We are committed to fostering a diverse and inclusive workforce.