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The Study Coordinator will join a collaborative and exciting team of researchers at the UCSF Francis I. Proctor Foundation studying eye diseases in the U.S. and internationally. Additionally, the Study Coordinator should have strong writing and communication skill as this employee will be responsible for supporting literature reviews, writing, editing, and formatting manuscripts, and managing and tracking the progress of manuscripts to high-impact medical journals.
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The study director will report to the Director of Study Oversight. represents the single point of control responsible for the overall conduct of a nonclinical laboratory study in accordance with Food and Drug Administration’s (FDA) Good Laboratory Practice (GLP) Regulations, 21 CFR Part 58 for the conduct of nonclinical laboratory studies.
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Partners with study abroad and African American Studies to coordinate the Annual Study Abroad Program. Coordinates and leads programming for the Ghana Study Abroad program and the HBCU exchange programs.
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The Study Director, Research Scientist will have a passion for preclinical research. Three years’ experience as a Study Director for in vivo studies (including GLP) in a biopharmaceutical company or Contract Research Organization (CRO) One to two years’ experience in Toxicology a plus.
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CDM Smith is currently seeking a GIS professional in various geographical locations to serve as flood risk study manager and quality reviewer in support of FEMA Risk MAP (Risk Mapping, Assessment, and Planning) activities nationwide.
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Responsible for managing relationships with CROs and other vendors for all study activities including study start-up, close out, and completion of Trial Master File. Responsible for collecting, preparing and reviewing regulatory documentation for IRB submission prior to study start-up.
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International experience including study abroad or work abroad. In this role, theAssistant Director is expected to work closely with a range of key stakeholders to help the WINS program flourish, including study abroad offices at partner institutions and prospective partners at visiting (non-WINS) institutions, Webster academic and enrollment management units, marketing and recruitment specialists, the Webster Division of Global Education leadership team, as well as international campus staff.
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OR A Ph. D. or equivalent doctoral degree in a related field of study such as: Sociology, Business Management, Business Administration, Public Administration, Social Science, Environmental Science, Geosciences, Political Science, Law Enforcement, or other fields related to the petroleum industry.
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The position will primarily support the new HEALthy Brain & Child Development Study (PIs Laurie Wakschlag & Elizabeth Norton, Scientific Project Director Renee Edwards), a national, consortium study looking at the impact of prenatal substance exposure and other adverse and protective factors on infant brain and behavioral development.
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Associate Principal Scientist, Statistical Programming - System Development Study Data Tabulation Model (SDTM)- Hybrid. BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus 9 years SAS programming experience in a clinical trial environment.
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PRN Home Study Specialist may also be responsible for the recertification of foster homes as determined by treatment director. As a Home Study Specialist, you will be responsible for the licensing of therapeutic foster parents as defined by annual goals.
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The Senior Clinical Study Manager (Sr. CSM) will independently organize and manage multiple activities related to clinical studies, while simultaneously ensuring study milestones are met and studies are completed in accordance with the protocol and ICH/GCP requirements.
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The Study Abroad Advisor provides administrative and operational support for all aspects of study abroad and exchange programs within the assigned portfolio. Familiarity with higher education systems, international education, and study abroad in the U.S.
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The Clinical Research Coordinator III position will be working on the Emory Healthy Aging Study and the Emory Healthy Brain Study ( The Emory Healthy Aging Study is an online longitudinal research study working to build a massive public health database to better understand how we age and age-related diseases.
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Responsibilities include establishment of, and adherence to, non-clinical study timelines, monitoring of study conduct at the TPO via communication with the Study Director and/or onsite observation, and real time communication with the Toxicology ADME/ToxPath/Drug Disposition (ATP) team throughout study planning, execution and reporting.
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study job Title: engineering manager Company: Skillz
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