IQVIA
Healthcare
ClinicalResearchCoordinator
“Clinical Research Coordinator at IQVIA. Skills: Clinical research, Participant advocacy, Study documentation. Support clinical research studies. Maintain safe study environment”
Industry & Context.
Short-term assignment (6 months), 20 hours per week
What They're Looking For.
Must Have
BSA in life sciences or equivalent education, Relevant work experience in clinical or medical setting, Knowledge of clinical trials, Proficiency in MS Windows, Proficiency in Microsoft Office applications
Nice to Have
Experienced Research Nurse, Highly experienced Clinical Research Coordinator, Highly experienced Site Research Assistant
What You'll Do.
Support clinical research studies
Maintain safe study environment
Safeguard participant well-being
Act as patient advocate
Address participant concerns
Maintain up-to-date study documentation
Plan logistical activities for study procedures
Coordinate logistical activities
Perform clinical study set-up
Perform clinical study preparation
Label specimen collection tubes
Label specimen containers
Manage inventory of supplies
Set up study equipment
Troubleshoot study equipment
Assist with data entry
Assist with data quality checks
Assist with query resolution
Support study enrollment activities
Ensure correct custody of study medication
Handle study medication
Coordinate with study monitors
Respond to monitor queries
Perform patient vital signs
Document patient vital signs
How You'll Work.
Team & Collaboration
Site team
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