- 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
- Teva Pharmaceuticals (West Chester, PA)
- …: Up to 10% Domestic **Location** : US-Based Remote (US Eastern time zone preferred ) **How you'll spend your day** + Writes and edits clinical regulatory documents ... (eg, study reports, protocols, briefing books, investigator 's brochures, health authority responses, Module 2.5 and 2.7.x)....Required: Bachelor's in life sciences or related field + Preferred : Master's, MD, PhD, PharmD Experience: + Required: 5+… more
- Mount Sinai Health System (New York, NY)
- …other assigned lab, as directed by the Laboratory Manager or Principal Investigator . **Qualifications** BS in Medical Technology or equivalent education to meet NYS ... DOH technologist standards. NYS Clinical Laboratory Technologist license required ASCP preferred or NCA certification preferred 0-1 year experience Collective… more
- Lilly (Indianapolis, IN)
- …staff, and investigators on protocols and data collection. - Participate in investigator identification and selection. - Ensure completion of ethical review board, ... a resource to monitors, investigators, and ethical review boards. - Review Investigator -Initiated Trial (IIT) proposals and publications. - Align Phase 3b/4 (and… more
- Wayne State University (Detroit, MI)
- …Essential functions (job duties): Under the direction of the Principal Investigator , provide scientific and technical assistance to complete laboratory based, ... staff with experiments /research protocols as required. Communicate with principal investigator and Postdoctoral scholars/fellows on the status of research. Collect… more
- University of Utah (Salt Lake City, UT)
- …to ensure uninterrupted project approval. 5. Tracks sponsor and investigator -initiated amendment notifications and submits amended protocols, summaries and consents ... study progress reports to the IRB . 7. Coordinates with study sponsor, investigator and IRB to complete study closure activities. 8. Assists investigators and others… more
- Dignity Health (Phoenix, AZ)
- …years the ALS Center researchers have conducted over 20 sponsored and investigator initiated clinical trials for ALS and Neuromuscular disorders with new research ... tracks and reports adverse events and deviations to the Investigator as well as the sponsor and IRB in...and/ or job-related experience in lieu of degree required. ** Preferred :** Three (3) years clinical research experience preferred… more
- Xeris Pharmaceuticals, Inc. (GU)
- …related to Xeris clinical research activity, including thought leader and investigator engagement and follow-up, and facilitation of unsolicited requests for ... interactions related to Investigator Initiated Studies (IISs). + Maintaining cross-functional collaboration with...(MD, PhD, PharmD, DNP) in a related discipline strongly preferred + Less than 2 years of experience [Entry… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …and assigned schedules. + Sets up experiments as prescribed by a principal investigator . + May be required to participate in laboratory maintenance activities such ... hazardous agents. + Performs related responsibilities as required by principal investigator . MINIMUM QUALIFICATIONS: + Bachelor's degree in a scientific field OR… more
- Magellan Health Services (Falls Church, VA)
- …human subject research, research subject protection, and institutional and investigator compliance. + Serves as point-of-contact for assigned Commands and ... with researchers, review of Command research files, and review of investigator files. Evaluate and assess findings objectively and integrate all activities… more