- United Therapeutics (Research Triangle Park, NC)
- …team and other stakeholders to provide biostatistical resources for investigator -sponsored clinical studies and address internal/external investigator queries ... expert input, conduct thorough reviews, and grant approval for submitted investigator -sponsored clinical studies, external investigator queries of UT databases,… more
- Tufts Medicine (Boston, MA)
- …to job area. **Job Overview** This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. Our ... and other endocrine conditions through a mix of industry-sponsored and investigator -initiated research studies. We're a close-knit group, made up of multiple… more
- Actalent (Lima, OH)
- …events (AEs) and Serious Adverse Events (SAEs) and promptly notify Principal Investigator and Sponsor. + Prescreen study candidates. + Obtain informed consent per ... ECGs, and other test results for completeness and alert values, ensuring investigator review in a timely fashion. + Discuss study medication, required procedures,… more
- Tufts Medicine (Boston, MA)
- **General Summary:** This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. Our Tufts ... to job area. **Job Overview** This position will assist the Principal Investigator (PI) in planning and implementing clinical research studies as assigned. **Job… more
- University of Michigan (Ann Arbor, MI)
- …as a Research Area Specialist Intermediate who will work alongside the Principal Investigator in the Department of Family Medicine and a team of investigators across ... study-related activities and help oversee project staff and milestones. The Principal Investigator and supervisor for this position in Dr. Kimberly McKee, an… more
- Astellas Pharma (Northbrook, IL)
- …planned clinical trials on assigned development programs (eg, develop protocols, investigator brochures, CRFs, informed consents, and clinical study reports and ... analysis for DMC/DSMB/DEC forums or regulatory submissions. + Provides training at investigator meetings and site initiation visits with clinical trial staff, and… more
- Cedars-Sinai (Beverly Hills, CA)
- …3days on campus, which are variable to accommodate patient visits, investigator schedules, study needs, meetings, staff coverage, audits/monitoring visits or ... protocol knowledge to serve as a liaison between nursing staff, Principal Investigator , other research staff, and study participants. Assists with the education of… more
- Dartmouth Health (Lebanon, NH)
- …with an increasing level of independence, working closely with the Principal Investigator (PI). The Clinical Research Coordinator II works under the supervision of ... the study operations (including subject management/regulatory) with oversight from the investigator or their designee. * Primarily supports subject management, such… more
- Cedars-Sinai (Beverly Hills, CA)
- …trial budgets for industry, National Institutes of Health (NIH), and investigator -initiated clinical research. Evaluates research protocols to assess resource needs, ... procedures, clinical research staff time, investigator time, and costs from ancillary departments. Determines cost...required. Bachelor's Degree Accounting, Finance, or other related degree preferred . + Minimum of 3 years of experience with… more
- University of Utah (Salt Lake City, UT)
- …control and completion of research studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in ... an understanding of research procedures; and the ability to function independently is preferred . Departments may require IRB CITI Course or IATA DGR training within… more