Clinical Research Coordinator II
On-siteLittle Rock, Arkansas, United States
Job Summary
Manage assigned clinical research studies by identifying and screening patients, conducting clinic visits, and performing direct care activities such as consenting, physical assessments, blood draws, and medication administration. Execute protocol adherence for randomization and enrollment while maintaining clean data entry, resolving IRB responses, tracking adverse events, and managing eSource materials. Ensure strict compliance with governing bodies and laws through productive site visits and efficient study maintenance. Communicate promptly with leadership, PIs, sponsors, and monitors to address corrections or questions.
Required Qualifications
- 3+ years of clinical research coordination experience
- legal authorization to work in the US
- strong desire to work directly with patients
- skilled in all aspects required for conducting an IRB approved clinical trial protocol: identification, screening, randomization, and enrollment of patients, conducting clinic visits, etc.
- skilled at performing and assisting with direct patient care activities: consenting patients, physical assessments, blood draws, medication administration, ECG, etc.
- acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
- expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
- ability to stay focused while running different protocols, resolving and submitting IRB responses and audit findings, tracking AE and SAE events, and maintaining eSource material for assigned studies
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