Clinical Research Coordinator II
On-siteColumbia, Missouri, United States
Columbia, Missouri, United StatesOn-siteFull TimeMedium
Full TimeMedium
Job Summary
Manage assigned studies and patients by conducting clinic visits, consenting, performing physical assessments, drawing blood, administering medication, and conducting ECGs. Execute protocol tasks including identification, screening, randomization, and enrollment while maintaining strict adherence to IRB-approved protocols and regulatory compliance. Ensure clean data entry, submit IRB responses, track adverse events, and maintain eSource materials. Communicate promptly with leadership, PIs, sponsors, and monitors to resolve issues and foster relationships.
Required Qualifications
- 3+ years of clinical research coordination experience
- A strong desire to work directly with patients
- A lover of patient interaction and skilled at providing patient care
- A team player with a bias for action and an attitude that takes personal responsibility
- 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.
- An acute attention to detail for clean data entry, regulatory compliance, productive site visits, efficient study set-up and maintenance, and strict protocol adherence
- An expert communicator with the goal of fostering relationships between the research team, PIs, Sponsors, Monitors, and others
- A strong advocate for Company values, mission, and initiatives
- Not easily distracted: You have the 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
- Energized by the idea of playing a role in the future of new therapy development in the areas of Gastroenterology, Urology, Dermatology, and/or Oncology
- Taking ownership of assigned studies and patients
- Communicating promptly and effectively with leadership and coworkers when you have a question or see something that needs correction
- Showing up on time, every time
- Ensuring strict compliance to the laws, regulations, and requirements of all applicable governing bodies
- Learning and using the technologies we provide to increase efficiency in your day-to-day activities
- Embodying our core values of Compassion, Integrity, Collaboration, Innovation, Velocity, and Dedication
- Legal authorization to work in the US
- Not currently accepting work visas
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