Clinical Monitor Jobs
Kelly - Rockville, MD, United States
The National Institutes of Health is seeking a Clinical Research Associate, Site Monitor . This is a long-term, full-time, contract position based in Rockville, MD. This position offers a competitive
from: linkedin.com - 6 days ago
ICON Strategic Solutions - , CA, United States (+1 location)
in this exclusive program. The Clinical Research Associate (CRA) monitors the progress of clinical studies at investigative sites or remotely, ensuring clinical trials are conducted, recorded, and reported
from: linkedin.com - 8 days ago
BAYADA Home Health Care - Monroe Township, United States (+5 locations)
across the continuum. Monitor clients' conditions; reporting changes to Clinical or Client Services Manager Follow up with, execute, and properly document doctors' orders Perform client assessments Case
from: us.lifeworq.com - 16 days ago
Scion Staffing - , CA, United States
) Monitor client caseloads to ensure that all bio-psychosocial assessments, individualized service plans, consents, and progress notes are promptly entered Plans and implement clinical training for staff
from: linkedin.com - 8 days ago
Charter Research - The Villages, FL, United States
Manager. Keep all source documentation up-to-date and in compliance with ALCOA-C standards. Communicate closely with the sponsor’s Clinical Research Associate (CRA) to facilitate the sponsor monitoring
from: linkedin.com - 8 days ago
ScionHealth - Hartsville, United States
more about our community here. Job Description: Performs plan of care intervention, including medication administration, assessments, specimen collection, clinical treatments, and other medical care
from: us.lifeworq.com (+1 source) - 12 days ago
SQRL - Chicago, IL, United States
investigational trial Management of the inventory; orders, replaces and returns study materials, as required. Assist in ensuring the participation of the pharmacy department in all clinical trials which involve
from: linkedin.com - 8 days ago
Medix™ - ST Louis, MO, United States
professionals to execute research protocols effectively. Regulatory Compliance: Ensure adherence to all relevant regulatory requirements, including FDA guidelines, IRB approvals, and Good Clinical Practice (GCP
from: linkedin.com - 8 days ago
ScionHealth - Livingston, United States
intervention, including medication administration, assessments, specimen collection, clinical treatments, and other medical care treatment. Documents patient care given. Monitors, records, and communicates
from: us.lifeworq.com - 12 days ago
Alliance for Clinical Trials in Oncology - Chicago, IL, United States
Purpose/Scope: The Clinical Trial Monitor will work under the Director of Industry Collaboration and Trial Management to oversee trial activity at sites participating in Alliance clinical trials
from: linkedin.com (+1 source) - 26 days ago
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