Clinical Research Coordinator II
On-siteFolsom, California, United States
Folsom, California, United StatesOn-siteFull TimeLicense Or CertificationMedium
Full TimeLicense Or CertificationMedium
Job Summary
Conduct patient screening, randomization, and enrollment for IRB-approved clinical trials while performing direct care activities such as consenting, physical assessments, blood draws, and medication administration. Manage assigned studies by tracking adverse events, resolving audit findings, maintaining eSource materials, and ensuring strict protocol adherence and regulatory compliance. Collaborate with leadership, investigators, and sponsors to foster relationships and communicate promptly on study corrections or questions.
Required Qualifications
- 3+ years of clinical research coordination experience
- strong desire to work directly with patients
- LVN license in state of CA
- Certified Medical Assistant
- injection experience
- legal authorization to work in the US
- ability to stay focused while running different protocols
- ability to resolve and submit IRB responses
- ability to track AE and SAE events
- ability to maintain eSource material for assigned studies
- ability to communicate promptly and effectively with leadership and coworkers
- ability to show up on time, every time
- ability to ensure strict compliance to the laws, regulations, and requirements of all applicable governing bodies
- ability to learn and use the technologies we provide
Desired Qualifications
- a strong advocate for Company values, mission, and initiatives
- 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
Hiring someone like this?
Get your role in front of qualified candidates on Sorce.