Nebraska Licensed Clinical Research Associate
A company is looking for a Clinical Research Associate to monitor and participate in clinical trials across the country for a leading Clinical Research Organization. Key Responsibilities Conduct site monitoring visits to ensure compliance with GCP, ICH, and regulatory guidelines Support subject recruitment and adapt recruitment plans as needed Track study progress, including regulatory approvals, enrollment, data collection, and query resolution Required Qualifications At least 2 years of onsite oncology monitoring experience Proficiency in CTMS, EDC, and Microsoft Office Suite Strong knowledge of GCP, ICH guidelines, and regulatory requirements Experience in site management, patient recruitment, and clinical trial documentation Bachelor's degree in life sciences, nursing, or a related field (advanced degree preferred)
A company is looking for a Clinical Research Associate to monitor and participate in clinical trials across the country for a leading Clinical Research Organization.
Key Responsibilities
Conduct site monitoring visits to ensure compliance with GCP, ICH, and regulatory guidelines
Support subject recruitment and adapt recruitment plans as needed
Track study progress, including regulatory approvals, enrollment, data collection, and query resolution
Required Qualifications
At least 2 years of onsite oncology monitoring experience
Proficiency in CTMS, EDC, and Microsoft Office Suite
Strong knowledge of GCP, ICH guidelines, and regulatory requirements
Experience in site management, patient recruitment, and clinical trial documentation
Bachelor's degree in life sciences, nursing, or a related field (advanced degree preferred)
