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If selected, you will play a significant role in the Disaster and Failures Studies (DFS) Program's Hurricane Ian Study program for roofing material evaluation, which includes working with NIST staff and external partners on planning and executing experimental research to study the effects of Hurricane Ian's wind hazards on roofing material, including asphalt shingles.
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Serve as a voting member on the Inotiv Gaithersburg Institutional Animal Care and Use Committee (IACUC) including study protocol submission review, veterinary study updates at monthly meetings, policy and guideline review, veterinary perspective, facility program review and inspections.
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Will play an instrumental role in performing biannual correlation study, documentation of quality controls, and maintenance for automated clinical microbiology instruments, performing the required proficiency survey and providing a summary of the conduct of this work in the annual report required.
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Strong technical and methodological skills (study design, data analysis, interpretation, communication) in clinical trials, epidemiology, or health services research, registries, Phase IV studies, technical peer review of HEOR research, observational study design and implementation is preferred.
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COMT, OCS, SCS, CSCS, Dry Needling, NCS, Pelvic Health, Oncology, and additional certifications PAID Specialty and special interest groups, study groups and more. We have a clinical team of PTs offering specialty services such as oncology, lymphedema, spine, pain management, ACL program, vestibular, work conditioning/hardening and MORE.
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Follow a spiritual rhythm including daily prayer and Bible study to seek the Lord's will for the ministry of FCA. Lead, conduct and provide spiritual leadership for staff, volunteers, coaches and athletes through prayer, Bible study, worship and living by example so they are equipped to serve others.
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Skilled scientist able to discern the advantages and fir fall of a range of analytical techniques such as molecular assays (ddPCR, qPCR, RT-qPCR), flow cytometry, ELISpot, viral assays, cytokine assays, ligand binding assays and Mass SpectrometryIn depth knowledge of concepts such of context of use of fit for purpose assay validation in bioanalysisOverseen assay transfer, scientific quality and study conduct at CRO partners.
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As required, set up Watson study designs based on a good understanding of various pharmaceutical studies and their designs and PDS SOPs and plans. Smithers PDS LLC (Pharmaceutical Development Services) assists in the development of new medicines by providing bioanalytical services for all phases of drug development from discovery through approval and post market surveillance.
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HEOR is responsible for providing a strong scientific perspective and contributing to HEOR study design and methodology, data analysis and aggregation, outcomes interpretation, and other activities across our research groups (strategic market access, modeling and meta-analysis, patient-centered outcomes, and real-world evidence), focusing primarily on strategic market access and modeling and meta-analysis.
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Work with the data manager and/or data scientists to plan and build database infrastructure for each research study Experience with performing statistical analyses for clinical and field-based research studies (e.g., intervention studies, epidemiological studies, patient-reported outcomes research and/or clinical outcomes research, etc.
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Consult with staff on the application of statistical methods to address the key study scientific aims of the study. Provide consultation to the staff on the use of statistical methods and software packages to address the key scientific aims of the study.
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Provide expert clinical operational input into: Target Product Profile (TPP), Clinical Development Plan (CDP), Study Synopsis, Clinical Study Protocol, Clinical Study Report, IB, briefing documents, etc., to ensure seamless delivery of programs through effective collaboration.
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O Manage activities related to study committees (CEC, DSMB/DMC, Independent Medical Monitor) or overseeing third party management of committee activities per study SMP and associated Charters.
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Assist with the collection of study data as required by the study protocol, specifically the CBH screening form, admission forms and release of information. Complete other study procedures such as weight/height, waist/hip circumference as specified on the appropriate flow sheets.
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Review study documentation with management to ensure completeness and ensure proper archival of trial-related materials. Work collaboratively with team members to ensure necessary information is cataloged, digitized, and archived at the end of a study.
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study job Company: National Gallery Of Art in Rockville, MD
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