- University of Utah (Salt Lake City, UT)
- …at the University of Utah has an immediate opening for a Clinical research coordinator . This position desires a person with a strong background in clinical research. ... and payment terms. 13. Maintain documents as required by FDA , ICH , GCP , and IRB regulatory...for trial completion. Review study related data to assure compliance with study protocol. This job description is not… more
- University of Utah (Salt Lake City, UT)
- …studies in an administrative and operational capacity while maintaining compliance with guidelines set by governing agencies. **Responsibilities** 1. Oversees ... compliance to protocol; manages quality control, completion and submission...research consortia. 7. Prepares, submits and maintains IRB , FDA , NCI , NIH , NSF and/or other… more
- University of Utah (Salt Lake City, UT)
- …submission, and experience in human subjects research. Must have a working knowledge of FDA , ICH , and other regulatory compliance ; an understanding of medical ... Summary** **VP Area** President **Department** 01345 - HCI Clinical Resrch Compliance **Location** Campus **City** Salt Lake City, UT **Type of Recruitment**… more
- University of Utah (Salt Lake City, UT)
- …Experience with human subjects research, good leadership skills, and working knowledge of FDA , ICH , and other regulatory compliance are also required. ... 1. Independently provides oversight for all aspects of study conduct, regulatory compliance , and record keeping processes at the site or institution level. 2.… more
- University of Utah (Salt Lake City, UT)
- …the University of Utah is looking for a Genetic Counselor Assistant. The coordinator will work closely with physicians, genetic counselors, and other staff to ... clinical information. 6. Follows techniques of clinical research coordination and practices, FDA Good Clinical Practices ( GCP ), and clinical research standard… more
- University of Utah (Salt Lake City, UT)
- …to operational execution-with a strong emphasis on patient safety, data integrity, and compliance . The ideal candidate will serve as a vital link between research ... or gene therapy settings. + Demonstrated experience with IND trials, FDA submissions, and managing multicenter or first-in-human studies is strongly preferred.… more
- Reckitt (Salt Lake City, UT)
- …+ Participate in and drive continuous improvement projects with EMOs. + Assures compliance with all cGMPs. + Liaise with cross functional teams to support key ... new or existing EMOs. + Effectively applies knowledge of FDA , and DEA guidelines. + Assists in the development,...impact of changes via Quality One or being change coordinator for new GICs and AWs. **The experience we're… more