- Edwards Lifesciences (Frankfort, KY)
- …and interpretation of results and also advise on the conduct of clinical studies , database development and data quality assurance with the analysis of clinical ... lead on one or more clinical trials, lead the coordination of analyses for study report and other documents and provide programming and validation support of these… more
- University of Southern California (Los Angeles, CA)
- …Pathology Core, etc) to identify potentially eligible participants and obtain study -related data. + Screening potential participants for eligibility and obtaining ... with team members and participating in regular team meetings to track study progress and coordinate schedules Successful Candidates Must Demonstrate: The successful… more
- Merck (North Wales, PA)
- …internal teams and external partners, design non-interventional and data synthesis studies , author study protocols, develop measurement questionnaires, case ... report forms, data analysis plans, final study reports, scientific presentations, and publications. + Responsible for study -related contracting, budgets, and… more
- Johns Hopkins University (Baltimore, MD)
- …will participate as a coauthor on manuscripts and presentations reporting study results. **Specific Duties & Responsibilities** + Use and expand existing ... JHHCC and CNICS data. + Identify potential problems with study data and collaborate with data managers to resolve...of results. + Document decision making during conduct of studies and archive code for purposes of reproducibility of… more
- Boston University (Boston, MA)
- …Gordon and Chris Wells, the fellow will play a central role in a multi-year study of public trust across New England. The project examines how residents of urban, ... ecologies people rely on. The successful candidate will contribute to a new study on local information ecosystems, which will employ the following methods. +… more
- AbbVie (Irvine, CA)
- …of the overall Product Development Plan. + Oversees project-related education of investigators, study site personnel and AbbVie study staff. + Responsible for ... and addressing applicable regulatory requirements related to the clinical studies , clinician reported outcomes, patient reported outcomes and global drug… more
- Access Dubuque (Dubuque, IA)
- …require that students work with hazardous materials while engaging in academic studies . Instructors of these courses and research projects must inform and train ... the hazards of specific chemicals that will be used during their course of study . Furthermore, instructors must enforce and follow safety policies. Prior to use of… more
- Access Dubuque (Dubuque, IA)
- …require that students work with hazardous materials while engaging in academic studies . Instructors of these courses and research projects must inform and train ... the hazards of specific chemicals that will be used during their course of study . Furthermore, instructors must enforce and follow safety policies. Prior to use of… more
- Access Dubuque (Dubuque, IA)
- …require that students work with hazardous materials while engaging in academic studies . Instructors of these courses and research projects must inform and train ... the hazards of specific chemicals that will be used during their course of study . Furthermore, instructors must enforce and follow safety policies. Prior to use of… more
- Huron Consulting Group (Chicago, IL)
- …you'll assist Huron's Research Office team in developing coverage analysis reports, study budgets, study calendars, charge segregation, and other trial ... documentation required for clinical research studies , including industry, federally sponsored, and locally (investigator) sponsored research. You will also assist in… more