- Sanofi Group (Cambridge, MA)
- …Director (CRD) in the medical/scientific contribution for the clinical studies on activities pertaining to the Study Medical Manager responsibilities ... late-stage clinical studies . The role requires close collaboration with Clinical Research Director (CRD) alongside other Study Team members : the Coding… more
- University of Miami (Miami, FL)
- …evaluating of multiple clinical research protocols. This role manages multiple studies ' daily operations, carries out study coordination duties from protocol ... study close-out according to regulatory/sponsor guidelines, assures each study 's integrity, and mentors less experienced Clinical ...authority logs, deviation logs, adverse event logs for all studies . + Assists PIs and study team… more
- Regeneron Pharmaceuticals (Warren, NJ)
- …and provision of clinical operations expertise during protocol design, feasibility, study start up and conduct phases of studies . Ensure consistency within ... quality, timelines and budgets related to the conduct of clinical research studies in accordance with applicable...with senior level management, external vendors, collaboration partners and clinical study personnel for clinical … more
- IQVIA (Norwich, CT)
- …support. **Scheduled Weekly Hours:** 34 hours **Job Overview:** Coordinate and participate in clinical research studies ensuring that studies are carried out ... to investigators to prepare for and execute assigned research studies + Reviews study protocols, source document...and other regulatory bodies governing the conduct of the study + Recruits and screens patients for clinical… more
- Abbott (Alameda, CA)
- …Study Lead as needed. + Proactively and effectively communicate the status of clinical studies to management. + Participate in the interim and final reviews ... clinical monitoring and site management activities, ensuring compliance to the Study Protocol, Good Clinical Practices (GCPs), ICH guidelines, Federal… more
- University of Pennsylvania (Philadelphia, PA)
- … clinical trials. Demonstrate knowledge of the federal regulations for the conduct of clinical studies and human subject protection. + Act in lead capacity in ... B: Bachelor's Degree with 2-3 years of related experience in research and clinical study methodologies or equivalent combination of education and experience is… more
- University of Utah (Salt Lake City, UT)
- …and English. This role focuses on serving as the site coordinator for a multi-site study clinical trial of insomnia treatment for midlife and older women. The ... leadership. ** Clinical Project Manager, I** Coordinate all aspects of clinical studies from initiation through delivery. Build and maintain relationships… more
- Stanford University (Stanford, CA)
- … trials research team and report to various Principal Investigators conducting clinical research. Responsibilities include preparation of initial study documents ... Clinical Research Coordinator Associate **School of Medicine, Stanford,...multiple research protocols assuring efficiency and regulatory compliance. These studies will be conducted at the Stanford Hospital and… more
- University of Utah (Salt Lake City, UT)
- …studies while assisting the Principal Investigator in determining and accomplishing study objectives. Oversees research studies in an administrative and ... followed. 13. Assists the Principal Investigator in the development of study protocols ** Clinical Research Coordinator (Non-R.N.), II** Coordinate day-to-day… more
- University of Pennsylvania (Philadelphia, PA)
- …quality of the clinical trial data and records, scheduling and conducting study initiation and monitoring visits, and participating in ongoing study protocol ... study data. Obtain records required to complete case report forms. Update/maintain study record in the Clinical Trials Management System (CTMS) in real-time.… more
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