- Charles River Laboratories (Ashland, OH)
- …Safety Assessment Group site located in **Ashland, Ohio.** Generate and record data with minimal supervision in the performance of studies. Responsible for handling ... and processing samples and performing accurate data collection and reporting. Perform laboratory tasks by various basic methods. + Perform basic laboratory… more
- J&J Family of Companies (Spring House, PA)
- …Chemistry, Urinalysis, and Blood Gas analyses to generate high quality data + Implementing innovative clinical pathology-based approaches and techniques to solve ... + Ensuring proper equipment maintenance, quality assurance, quality controls, data and data preparation for archiving +...skills are required + Strong skills related to time management , attention to detail and documentation are required +… more
- Takeda Pharmaceuticals (Boston, MA)
- …assessment strategies for products. + Oversees signal detection and risk management activities for assigned products and ensures that development plans include ... business and departmental needs + Leads PSPV Safety Team (GST) and Safety Management Team (SMT) for assigned GI compounds and products. + Represents the… more
- Fujifilm (Holly Springs, NC)
- …Spectrophotometry, Mass Spectrometry. * Experience using quality systems (eg, deviation management system, change control , corrective and preventive action ... Relationship Management * Experience using quality systems (eg, deviation management system, change control , corrective and preventive action (CAPA),… more
- Charles River Laboratories (Malvern, PA)
- …responsible for providing relevant support and analysis to Client Project Management , Project Coordination, and Business Operations, necessary to achieve a ... of these responsibilities includes, but is not limited to, cost center expense management , invoice review and sign-off, analysis and management of the site's… more
- Loyola University Chicago (Chicago, IL)
- …Responsibilities The Clinical Research Coordinator II is responsible for the overall management and implementation of an assigned set of multiple research protocols ... accordance with good clinical practice guidelines. Collect, record and maintain complete data files using good clinical practice in accordance to HIPAA regulations.… more
- University of Florida (Gainesville, FL)
- …Allied Health, Nursing, Health Care Administration/Support Department: 27320505 - HA-UFHCC CRO EXP THER Classification Title: Clinical Research Coordinator II / ... of human clinical trials. + Interpreting and collecting medical and clinical data for prospective and existing enrolled subjects on assigned clinical trials. +… more
- University of Pennsylvania (Philadelphia, PA)
- …Organize and maintain all documentation required by the Investigator, sponsor or CRO , includes source documentation, case report forms, and research charts. Collect, ... review and report study data . Complete case report forms and resolve ...and queries with input from a supervisor as required. Management of clinical trials and will need to use… more
- University of Pennsylvania (Philadelphia, PA)
- …Organize and maintain all documentation required by the Investigator, sponsor or CRO , includes source documentation, case report forms, and research charts. Collect, ... review, and report study data . Complete case report forms and resolve ...The CRC B will have less supervision in the management of clinical trials and will need to use… more
- Actalent (Waltham, MA)
- …programming activities across various studies and programs, ensuring high-quality clinical data and analysis are delivered timely and within budget. Responsibilities ... third-party teams. + Oversee contracted vendors or vendor groups within CROs to ensure data and analyses are complete, accurate, and delivered on time. + Monitor and… more
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