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Administrative Support Coordinator II Job No: 537389 Work Type: Locations: San Diego Categories: Unit 7 - CSUEU - Clerical and Administrative Support Services, Administrative, Probationary, Full Time, On-site (work in-person at business location) Position Summary The Administrative Support Coordinator II is a staff member of the Fowler College of Business assigned to the Finance, Management and Marketing (FMM) department office.
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The Clinical Informatics Specialist 3 - Epic Reporting is responsible for triaging, designing, managing, and meeting analytics needs across the UCSD Health system. The Clinical Informatics Specialist 3 - Epic Reporting is responsible for producing reports in Reporting workbench, Radar, Clarity, Crystal and Tableau.
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Certification as a Clinical Research Coordinator. Coordinate research efforts with the Moores Cancer Center team through close communication and collaboration with the Associate Administrative Director and Administrative Director.
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Previous work experience on computers and experience with MS Word, Excel, OutlookMust have strong organizational and prioritization skills with previous administrative work experience. Creating power point presentations for departmental meetings, scheduling departmentalContribute and focus on the daily growth of the operation through awareness and understanding of LQA, EES, Forbes, Ecosure and Fairmont Grand Del Mar StandardsWork in conjunction with the Executive Chef, Food & Beverage Director and Outlet Chef on promotions, menus, and special events.
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As a reminder the folks who work with us come from a wide variety of backgrounds like customer service representative, administrative assistant, health care workers, human resources, warehouse workers, car delivery drivers, remote work from home professionals, and many more.
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Under the supervision of the Site Director, the Clinical Research Coordinator I is responsible for the conduct of research protocols, such that the integrity and quality of the clinical research is maintained and the research is conducted in accordance with Good Clinical Practice Guidelines.
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The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to coordinate and/or implement the study. Works with a Clinical Research Coordinator, Research Program Administrator or Research Nurse to coordinate/implement study.
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Experience as an ophthalmic technician and/or coordinator in the field of ophthalmology. Working knowledge of clinical or laboratory research, clinical trial recruitment, eligibility, protocol adherence, quality data submission and adverse event reporting.
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In this position, you will work closely with other Immunization program team members, including the Provider Quality Assurance (PQA) nurses, Storage and Handling team, Ordering Specialists, and Provider Education Coordinator to support all aspects of federal vaccine program for participating providers.
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The Lab Coordinator will report to a Lab Supervisor and will be responsible for helping with the laboratory glassware cleaning, restocking, organizing, and maintenance of the GMP (Good Manufacturing Practices) analytical, formulation, and product containment laboratories.
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Develops, implements, and automates business and reporting solutions by working with stakeholders in their design, planning, and implementation while ensuring consistency and coherency; summarizing data and results; creating summary statistics; organizing data reports, visualizations, and/or interactive Business Intelligence (BI) reports; identifying needs for the development and implementation of additional reporting solutions; and preparing documentation as appropriate.
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The Clinical Safety Scientist will provide operational and scientific support in managing the development, implementation and oversight of Arrowhead investigational products with engaging in, but not limited to: support safety governance and surveillance procedures including safety reporting processes, advanced safety analytics, expedited and periodic aggregate reports ensuring compliance with internal standard operating procedures, FDA and global safety reporting requirements.
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The Associate Director, PK and Bioanalysis at Pharmaron, will play a pivotal role in directing the scientific aspects and processes of in vivo pharmacokinetic studies, inclusive of bioanalysis and comprehensive reporting of noncompartmental PK parameters.
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Provide leadership, support and prioritization of all system enhancement requests of key P&P systems including Workday (HCM Core, Compensation, Performance Management, Reporting, Benefits, Absence, and Talent Development modules) and system integrations such as Greenhouse (ATS), Cornerstone (LMS), recognition platforms, etc.
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Rudolph & Sletten, a Tutor Perini Company, is seeking a Proposal/Marketing Coordinator to join our office in CA.About Rudolph & Sletten:In the last six decades, Rudolph and Sletten has built thousands of projects across our five California offices, from research centers designed to cure diseases to institutions that educate future generations to civic facilities and high-tech campuses that move our state forward.
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administrative coordinator reporting jobs in San Diego, CA
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