- ICON Clinical Research (Salt Lake City, UT)
- …+ Assisting in the planning, implementation, and coordination of clinical research activities in accordance with study protocols, regulatory guidelines, and ... preferably in a research or academic healthcare setting, with exposure to clinical trial operations and Good Clinical Practice (GCP) guidelines. +… more
- ICON Clinical Research (Winston Salem, NC)
- …a vital role in designing, conducting, and reporting nutrition-related clinical trials . This position blends patient care, research methodology, and data ... where you'll play a key role in transforming the clinical trial experience for patients and sponsors...Salem, Salisbury, Hickory Responsibilities: + Design & implement nutrition-related clinical trials , developing research protocols,… more
- ICON Clinical Research (Mount Pleasant, SC)
- Clinical Research Coordinator - Level 2 ICON...inclusion and exclusion criteria for each participant during the trial for their trials as well as peer ... plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster...strong relationships with Investigators and provides ongoing communication about trial status and participants * Dispenses study … more
- ICON Clinical Research (Wilmington, NC)
- Clinical Research Coordinator ICON plc is a...where you'll play a key role in transforming the clinical trial experience for patients and sponsors alike. ... world-leading healthcare intelligence and clinical research organization. We're proud to foster...effectively selling our service to suitable patient participants for clinical trials with set time allotted each… more
- ICON Clinical Research (Raleigh, NC)
- Clinical Research Coordinator Nurse - Raleigh,...where you'll play a key role in transforming the clinical trial experience for patients and sponsors ... (Onsite) ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster...**What you will be doing:** + Coordinating and conducting clinical trial procedures according to protocol requirements… more
- ICON Clinical Research (Charleston, SC)
- As a Clinical Research Associate you will be joining the world's largest & most comprehensive clinical research organisation, powered by healthcare ... doing:** + Conducting site qualification, initiation, monitoring, and close-out visits for clinical trials . + Ensuring protocol compliance, data integrity, and… more
- Mount Sinai Health System (New York, NY)
- …for investigators, sponsors, IRB, and institutional leadership on psychiatry research studies . * Oversee development of study protocols, case report forms ... (SOPs). * Supervise, mentor, and evaluate clinical research coordinators and assistants supporting psychiatric trials .... research coordinators and assistants supporting psychiatric trials . * Monitor and report on study … more
- Mount Sinai Health System (New York, NY)
- …The **Project Manager II** will oversee the entire portfolio of Investigator-Initiated Clinical Trials (IICTs)/ Clinical Research Sponsor Collaboration ... implementing, and overseeing comprehensive training programs for new staff within the clinical research teams. This role ensures that new employees are… more
- Stanford University (Stanford, CA)
- …strategies for promoting/recruiting research participants and retaining participants in long-term clinical trials . + Oversee data management for research ... Clinical Research Coordinator 2 - GI...complex projects and assignments. This role primarily involves overseeing clinical trials ranging from nonalcoholic steatohepatitis (NASH)/metabolic… more
- University of Pennsylvania (Philadelphia, PA)
- …help accelerate this momentum through the conduct of cutting-edge clinical trials . Job Description Clinical Research Coordinator B Responsibilities This ... and overseeing the quality of the clinical trial data and records, scheduling and conducting study...immunotherapies, etc.) Phase I - IV clinical trials and registries within the ACC CRU Research… more