Clinical Research Associate - Regulatory & IRB
Rutgers University–New Brunswick
Rutgers University is looking for a Clinical Research Associate at the New Jersey Medical School in Newark, NJ. This role involves working within a multidisciplinary research team, ensuring compliance with regulatory guidelines and Institutional Review Board standards. The ideal candidate will possess a Master's degree and have at least three years of research experience, including two years in university-level regulatory affairs. Responsibilities include coordinating regulatory compliance and preparing documentation for grant submissions. #J-18808-Ljbffr
- ...University of New Jersey, is seeking a Clinical Research Associate in the Department of Medicine within... ...in human subjects protection, regulatory guidance and coordination with Institutional... ..., OHRP, HIPAA, Conflict of Interest, IRB and institutional guidelines, and...RegulatoryWork at office
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$105.4k - $132.5k
...Clinical Research Associate Facility: Clinical Development Location: Plainsboro, NJ, US About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. From healthcare...RegulatoryLocal areaRemote workFlexible hoursNight shiftWeekend work- ...service they deserve. Job Description: As an Oncology Clinical Research Assistant (CRA), you will be assisting team members at... ...work efficiency and productivity. Assisting Regulatory Specialist (RS) on IRB submissions and interact to maintain regulatory documents...RegulatoryFull timeLocal area
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$105k - $115k
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...related to evidence-based recommendations in accordance with the Association for the Health Care Environment (AHE), Association for... ...operative Nurses (AORN), CDC, The Joint Commission, and other regulatory bodies. Maintains supplies and equipment by properly stocking...RegulatoryFull timePart timeMonday to Friday- ...A prominent educational institution in New Jersey seeks an Associate Director for Clinical Research to lead clinical research activities, oversee human research services, and coordinate scientists. The ideal candidate will possess an MD or equivalent, international recognition...
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$180k - $200k
...The Hut Group is seeking a Quality Director to lead the global Quality, Compliance, and Regulatory strategy for its beauty brands. The ideal candidate will have extensive experience in quality leadership within cosmetics or dietary supplements, deep knowledge of global...Regulatory- ...Responsibilities Member of the clinical team responsible for conducting Phase I-IV single or multi center studies according to Federal... ...planning study conduct, designing case report forms (CRFs), Contract Research Organization (CRO) selection and management, selection and...Contract work
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$110k - $140k
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$25 - $30 per hour
...inspections by preparing documentation, records, and operational evidence. Coordinate chemical and biohazard waste disposal following regulatory and safety guidelines. Work cross-functionally with QA, facilities, and safety teams to maintain lab readiness. Install,...Regulatory- ...applications. The role involves collaborating with various stakeholders to gather business requirements and ensure compliance with regulatory standards. Ideal candidates will have over 10 years of experience in the industry, working with tools like JIRA and SharePoint,...Regulatory
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