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Description: Position Summary The Project Manager Assistant (PMA) performs a variety of research and administrative duties to support the management of clinical trials at the Duke Reading Center (DRC) for which the DRC serves as the imaging core...
Description: Looking to hire an individual with a Clinical Research Coordinator background to act as a consultant CRC to a research site conducting a clinical trial. This CRC will support various parts of the study including patient recruitment,...
Job Title: Clinical Research Assistant - Full-time, Travel Required Department: Clinical Nutrition Shift: 1st Specialty: Research Job Number: 2 Date Posted: 07/06/2022 Position Type: Research Job Qualifications: Clinical Research Assistant Job Summary:...
Job Title: Medical Assistant - Rush - Lisle Cancer Center - FT, $2,000 BONUS! Department: Hematology/Oncology Shift: 1st Specialty: Hematology Job Number: 2 Date Posted: 08/08/2022 Position Type: Clinical Support Staff Job Qualifications: Medical...
Job Title: Phlebotomist - Inpatient Part time 1st shift Department: RML Customer Service Shift: 1st Specialty: Phlebotomy Job Number: 2 Date Posted: 08/03/2022 Position Type: Laboratory Services Job Qualifications: RUSH UNIVERSITY MEDICAL CENTER JOB...
Description: - Level 3 trauma center - Maternity unit and Level 2b nursery. - We have all generalists that keep moving throughout the lab on their shift. - Our lab is noted for the fast TAT on ED testing, all ED tests completed within 30 minutes (45...
These positions will start remotely, then are expected to be on-site 3-4 days per week. Preferred Qualifications: Previous experience with therapeutic clinical research involving drugs and/or devices. Experience in Phase I, II, and III clinical research....
Description: • The role will support day-to-day management of both short- and long-term department and client projects from start to finish in alignment with company Site Management Organization (SMO) and Academic Research Organization (ARO) strategic...
Description: Conduct and manage clinical trials in accordance with the study protocol, GCP, ICH Guidelines and SOPs • Coordinate, with supervision, assigned clinical trials including start up, vendor management, subject recruitment, source development...
Description: Auditing • Independently leads the planning, conducting, and reporting of assigned GCP QA routine and non-routine GCP audits including Clinical Investigator Site, Trial/Program, External Service Provider, Process/System and Local Operating...