Senior Clinical Research Associate
Behavioral Health Market Context
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Job Description
t as a liaison between study teams and site staff
Required Qualifications
Minimum of 3 years of recent on-site monitoring experience, including oncology trials
Experience supporting studies across multiple therapeutic areas, including general medicine
Working knowledge of CTMS, EDC platforms, and Microsoft Office tools
Strong understanding of GCP, ICH guidelines, and clinical research regulations
Bachelor's degree in life sciences, nursing, or a related discipline (advanced degree preferred)
Required Qualifications
Minimum of 3 years of recent on-site monitoring experience, including oncology trials
Experience supporting studies across multiple therapeutic areas, including general medicine
Working knowledge of CTMS, EDC platforms, and Microsoft Office tools
Strong understanding of GCP, ICH guidelines, and clinical research regulations
Bachelor's degree in life sciences, nursing, or a related discipline (advanced degree preferred)
Qualifications
- •Minimum of 3 years of recent on-site monitoring experience, including oncology trials
- •Experience supporting studies across multiple therapeutic areas, including general medicine
- •Working knowledge of CTMS, EDC platforms, and Microsoft Office tools
- •Strong understanding of GCP, ICH guidelines, and clinical research regulations
Benefits
Responsibilities
- •Perform on-site and remote monitoring visits to ensure compliance with GCP, ICH, and regulatory standards
- •Collaborate with investigative sites to enhance enrollment efforts and modify recruitment strategies as needed
- •Deliver protocol-related training and act as a liaison between study teams and site staff
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