- University of Utah (Salt Lake City, UT)
- …Independently performs all on-site or remote monitoring activities. **Responsibilities** Monitors clinical studies in accordance with FDA regulations, ICH ... teams and study Investigators. Provides guidance for appropriately returning the clinical study to full regulatory compliance. Works directly with Principal… more
- Edwards Lifesciences (Columbus, OH)
- … subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/ study safety, in keeping with protocols, GCP (Good ... be part of our inspiring journey. As the Senior Clinical Research Monitor , you will ensure trial...make an impact by ** * Field monitoring of studies and data collection for clinical trials,… more
- Edwards Lifesciences (Columbus, OH)
- … subject documentation is within parameters of study hypothesis, as well as to monitor clinical trial/ study safety, in keeping with protocols, GCP (Good ... be part of our inspiring journey. As the Senior Clinical Research Monitor , you will ensure trial...make an impact by ** * Field monitoring of studies and data collection for clinical trials,… more
- Johns Hopkins University (Baltimore, MD)
- …Title: Sr. Compliance Monitoring Specialist Job Posting Title (Working Title): Clinical Research Monitor Role/Level/Range: ACRP/04/MD Starting Salary Range: Min ... The Department of Neurology is seeking a **_Clinical Research Monitor (CRM)_** who will take the lead on compliance monitoring of predominantly large,… more
- UTMB Health (Galveston, TX)
- Clinical Study Monitor -...findings from monitoring visits. + Asses the conduct of clinical studies by monitoring compliance with the ... research. **Job Summary:** Monitors the administrative components and progress of clinical research studies approved by UTMB Institutional Review Board (IRB).… more
- Beth Israel Lahey Health (Boston, MA)
- … Clinical Trials Monitor (CTM) monitors and audits the investigator-initiated clinical research studies across all disease groups in the Cancer ... with GCLP and ICH guidelines. (essential) + Conducts detailed review of clinical studies in collaboration with pharmaceutical companies and other sponsors.… more
- University of Southern California (San Diego, CA)
- …Conduct onsite and remote monitoring for assigned clinical sites and co- monitor visits. Review Investigator Site Files, study data, perform IP ... trials. Incumbent will provide oversight to the progress of clinical trials at study sites, and ensure... protocol and manuals. + Work closely with Lead Clinical Monitor /Lead CRA to escalate site compliance… more
- Johns Hopkins University (Baltimore, MD)
- …member of Interstitial Lung Disease (ILD) Team to care for patients with ILD. The Clinical Nurse will work under the supervision of an attending ILD physician who is ... and pulmonary fellows. **Specific Duties & Responsibilities** _Clinical_ + Monitor and follow-up on diagnostic test results, prescriptions, medical equipment,… more
- Stanford University (Stanford, CA)
- …of a large study or all aspects of one or more small research studies . May include the supervision of clinical research staff. Duties include: + Oversee ... strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials. + Monitor and oversee data management for… more
- Stanford University (Stanford, CA)
- …for staff handling research administration activities associated with the conducting of clinical trials. Monitor staffing levels and identify adequate coverage ... Clinical Research Manager **School of Medicine, Stanford, California,... Research Manager will provide leadership and oversight of studies conducted by several affinity groups within the Department.… more
- University of Pennsylvania (Philadelphia, PA)
- …Cancer Center Department of Operations, Compliance and Monitoring (DOCM) is seeking a clinical research monitor /auditor to support our clinical research ... or related field preferred. Minimum of seven years of experience as a clinical research monitor /auditor, research nurse or research coordinator with at least… more
- Stanford University (Stanford, CA)
- …for staff handling research administration activities associated with the conducting of clinical trials. Monitor staffing levels and identify adequate coverage ... Department Clinical Research Manager **School of Medicine, Stanford, California,...for trial workload across teams of study coordinators. + Supervise the implementation of and adherence… more
- Bristol Myers Squibb (Trenton, NJ)
- …and CRA training materials and presentation at SIVs and Investigator meetings. + Review clinical narratives + Monitor clinical data, issue and resolve data ... queries + Monitor clinical data for specific trends + Develops Data Review...point of contact for clinical questions + Clinical contributions to clinical study … more
- Stanford University (Stanford, CA)
- …for staff handling research administration activities associated with the conducting of clinical trials. + Monitor staffing levels and identify adequate coverage ... Network Clinical Research Manager (Hybrid), Cancer Center South and...for trial workload across teams of study coordinators. + Audit operations, including laboratory procedures, to… more
- CUNY (New York, NY)
- … rotations - Develop student evaluation instruments consistent with the goals of each clinical rotation - Monitor the receipt of all components and assessment ... has a Master of Science degree in Physician Assistant Studies (PA). Our PA Program is a 28-month graduate...instruments on Typhon System - Grade medical notes - Monitor individual student progress during the clinical … more
- Bristol Myers Squibb (Madison, NJ)
- …Clinical Scientist function provides scientific expertise necessary to design and deliver clinical studies and programs. Position Summary / Objective + Will ... present these at SIVs and Investigator meetings + Review clinical narratives + Monitor clinical ...the protocol in collaboration with Data Management/Programming + Submit clinical contributions to clinical study … more
- Colgate-Palmolive (Piscataway, NJ)
- …based in our Piscataway, New Jersey location. **Responsibilities:** + Coordinate internal and external clinical studies . + Monitor the conduct of external ... industry and advanced degree or lab research acceptable). + Moderate experience in clinical research ( study design and/or execution, clinical methodologies,… more
- University of Miami (Miami, FL)
- …Division faculty + Develop protocols and implement patient safety initiatives to improve clinical outcomes + Monitor quality and appropriateness of medical care, ... Reproductive Sciences has an exciting opportunity for an Associate Professor of Clinical , General Division Chief. The incumbent will serve as an attending physician… more
- State of Georgia (Gwinnett County, GA)
- …for each student in a timely manner. . Guide students in completing required clinical paperwork. . Monitor clinical assignments to assure each student ... Instructor- Clinical Coordinator Diagnostic Medical Sonography Georgia - Gwinnett...accreditation policies and guidelines. + Assist in conducting a self- study of the program's compliance with technical college, program… more
- WuXi AppTec (Austin, TX)
- …within the Operations team and is assigned as a study lead to manage clinical trial studies . The Senior CRA will partner with a Project Manager to support ... Senior CRA will work to manage, oversee and may monitor /co- monitor clinical trial sites. **Essential...teams, liaise with other functional areas to accurately coordinate clinical study activities + Coordinate clinical… more