- University of Utah (Salt Lake City, UT)
- …Yes **Type** Non Benefited Staff / Student **Temporary?** Yes **Standard Hours per Week** 19 **Full Time or Part Time ?** Part Time **Shift** Day ... **Priority Review Date (Note - Posting may close at any time )** **Job Summary** **Clinical Research Coordinators (Non-R.N.)** This position is patient-sensitive… more
- University of Utah (Salt Lake City, UT)
- …**FLSA Code** Administrative **Patient Sensitive Job Code?** Yes **Standard Hours per Week** 40 **Full Time or Part Time ?** Full Time **Shift** Day ... **Work Schedule Summary** This position requires full- time in-office presence for up to six months, or...standards, including managing IRB protocols and assisting the Principal Investigator with NIH reporting. * Adhere strictly to ethical… more
- University of Utah (Salt Lake City, UT)
- …**FLSA Code** Administrative **Patient Sensitive Job Code?** Yes **Standard Hours per Week** 40 **Full Time or Part Time ?** Full Time **Shift** Day ... Date** 01/21/2026 **Priority Review Date (Note - Posting may close at any time )** **Job Summary** **Job Summary** The Department of Pediatrics, Division of Pediatric… more
- Ventura County (Ventura, CA)
- …of Motor Vehicles printout (K4 - 10-year driving record) to the Background Investigator . CONDITIONAL OFFER OF EMPLOYMENT: Certified candidates may receive ... TIME OF FILING. The supplemental questionnaire is considered part of the application and may be used throughout...Law, and poor neighborhood reputation. 13. Dishonesty during any part of the application, background investigation, or… more
- University of Utah (Salt Lake City, UT)
- …**FLSA Code** Administrative **Patient Sensitive Job Code?** Yes **Standard Hours per Week** 40 **Full Time or Part Time ?** Full Time **Shift** Day ... 12/31/2025 **Priority Review Date (Note - Posting may close at any time )** **Job Summary** Coordinates the implementation, quality control and completion of research… more
- University of Utah (Salt Lake City, UT)
- …**FLSA Code** Administrative **Patient Sensitive Job Code?** No **Standard Hours per Week** 40 **Full Time or Part Time ?** Full Time **Shift** Day **Work ... Date** 02/23/2026 **Priority Review Date (Note - Posting may close at any time )** **Job Summary** Develops and coordinates the submission of regulatory documents for… more
- Lilly (Indianapolis, IN)
- …articulate associated tradeoffs in value (data generated, risks created/discharged, cost, and time ). + Represent program and trial design optionality to asset teams ... impact of study/protocol design features to feasibility, value, patient and investigator burden, and execution speed/efficiency. + Engages other functions as… more
- J&J Family of Companies (Irvine, CA)
- …study protocol, informed consents, CRF, monitoring plan, study manual, investigator brochure, annual reports), ensure registration on www.clinicaltrials.gov from ... and company personnel; + Supervise the development and execution of Investigator agreements and trial payments; + Responsible for clinical data review… more
- Lilly (Indianapolis, IN)
- …and review of clinical / regulatory documents (eg, protocols, Investigator Brochures, clinical study reports, briefing packages, etc.); collaborates ... clinical data in internal and external meetings, as needed (eg, DSMB, training, Investigator meetings, Board presentations, etc.) + Other duties as assigned or as… more
- J&J Family of Companies (Danvers, MA)
- …candidates will be located near a major airport and have a strong clinical background in procedural areas. The Field Research Specialist is a dual-role position that ... and parlaying clinical trial experience, knowledge, and feedback ("Voice of Investigator ") to Abiomed cross-functional partners such as R&D, medical affairs,… more