Clinical Research Coordinator II
On-siteSt. Louis, Missouri, United States
St. Louis, Missouri, United StatesOn-siteFull TimeMedium
Full TimeMedium
Job Summary
Conduct full-cycle patient screening, randomization, and enrollment for IRB-approved clinical trials across Gastroenterology, Urology, Dermatology, and Oncology. Perform direct patient care activities including consenting, physical assessments, blood draws, medication administration, and ECGs. Maintain clean data entry, manage eSource materials, track adverse events, and resolve IRB responses and audit findings. Ensure strict protocol adherence and regulatory compliance while communicating effectively with PIs, sponsors, and monitors.
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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