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ALL ABOUT TARGET As part of our collaborative and guest-obsessed team, you help us create an experience that makes guests say, “I love Target!” When you work at Target, you’re helping ..
:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Compliance Analyst – Professional Services supports the efforts of the Revenue Cycle Compliance component of the UCSF Healthcare Compliance Program through adherence and promotion of functions which correspond ..
:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Compliance Educator supports the efforts of the Revenue Cycle Compliance component of the UCSF Healthcare Compliance Program through adherence and promotion of functions which correspond to the seven ..
A law firm in San Francisco is seeking an FDA Regulation Associate Attorney with 5-10 years of broad experience in counseling companies with FDA-regulated products. The successful candidate will be responsible ..
Senior Regulatory Affairs Manager The candidate is ... a key member of the Regulatory Affairs team and will lead ... and will lead the daily regulatory operations and compliance for..
... control to ensure we meet regulatory standards, and procure the needed ... consisting of colleagues from commercial, regulatory, supply chain, manufacturing and quality. ... integrated plans across Technical Operations,..
:text,ActualValueFromSolar:null},{QuestionName:Recruiter,AnswerValue:Yvonne Seminario,VerityZone:recruiterid,QuestionType:Multi-Select,ActualValueFromSolar:null},{QuestionName:Opportunity Overview,AnswerValue:u003cspan style=font-family:Arial,Helvetica,sans-serif;\u003eu003cstrongu003eIf you’re looking for a challenging and rewarding career,u003c/strongu003e the Registered Branch Associate role at Edward Jones may be the right opportunity for you. Registered Branch Associates create ..
Who We Are From research and discovery to post-market clinical development, our WWRD engine involves all bench and clinical research and the associated groups that support those endeavors. Our teams work ..
Environmental Regulatory Associate The candidate involves support for our clients on a broad array of issues such as market access; product development and premarket approval; responsible sourcing, supply chain, and transactional ..
Who We Are For more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were ..
Bio-Rad Clinical Diagnostics Group (CDG) is one of the leading global providers of tests for infectious and autoimmune disease screening, diabetes screening and monitoring, blood grouping as well as a whole ..
... control to ensure we meet regulatory standards, and procure the needed ... with Clinical Operations, QA and Regulatory to develop kits and label ... for clinical trial material packaging,..
... lives. Responsibilities Analyst role for Regulatory Research & Intelligence (RRI) includes: ... Intelligence (RRI) includes: Supporting senior regulatory research staff involved in examining ... research staff involved in examining..
:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eReporting to the Director of Revenue Cycle Compliance, the Associate Director of Revenue Cycle Compliance u0026 Audit is responsible for developing, implementing and leading the compliance initiatives of the ..
... patients. SUMMARYThe Associate Director of Regulatory Global Labeling (REG-GL) is a strategic role ... the development and management of labeling for products worldwide. Responsibilities may ... worldwide. Responsibilities may..
Job ID 21000KNEAvailable Openings 1PURPOSE AND SCOPE: Supports FMCNA’s mission, vision, core values and customer service philosophy. Adheres to the FMCNA Compliance Program, including following all regulatory and FMS policy requirements. ..
:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Research Compliance Analyst reviews clinical research protocols, Informed Consent Forms, Clinical Trial Agreements, and other relevant study-related documents. S/he determines what protocol-driven items, procedures and services are billable ..
:,ActualValueFromSolar:null},{QuestionName:Job Summary,AnswerValue:JOB OVERVIEWu003cbr/u003eThe Senior (Sr.) Compliance Educator supports the efforts of the Revenue Cycle Compliance component of the UCSF Healthcare Compliance Program through adherence and promotion of functions which correspond to ..
... of US, EU, and International labeling for commercial products.u00A0 The incumbent ... responsible for assessing and managing labeling changes for lifecycle products and ... lifecycle products and develop new..
... control to ensure we meet regulatory standards, and procure the needed ... written technical reports, contributes to regulatory submission documentsu00A0Contributes to the overall ... have a broad knowledge of..
Who We AreFor more than two decades, going our own way has led to countless breakthroughs, bettering the lives of those suffering from rare genetic disease. In 1997 we were founded ..