ICON Clinical Research is seeking a Senior Clinical Trial Transparency Associate to ensure compliance with clinical trial transparency regulations and enhance the visibility of clinical trial processes. The position is fully remote, emphasizing collaboration across teams and adherence to regulatory standards
Job Summary
As a Senior Clinical Trial Transparency Associate at ICON Plc, you will be instrumental in ensuring the transparency and integrity of clinical trial data and results.
You will be responsible to plan, lead and coordinate activities for submissions documents related to redaction/anonymization activities for Health Canada PRCI and EMA Policy 0070.
ICON offers a range of additional benefits designed to be competitive within each country and focused on well-being and work life balance opportunities.
Matching Summary
Match Score: 85
ICON Clinical Research is seeking a Senior Clinical Trial Transparency Associate to ensure compliance with clinical trial transparency regulations and enhance the visibility of clinical trial processes. The position is fully remote, emphasizing collaboration across teams and adherence to regulatory standards.
Skills & Requirements
Must-have
clinical trial transparency regulations
document anonymization
Health Canada PRCI
EMA Policy 0070
clinical trial data reporting
Nice-to-have
foster an inclusive environment
driving innovation and excellence
high standards of clinical trial reporting
effective relationships with regulatory bodies
Key Requirements
Advanced degree in life sciences, public health, or law
Extensive experience in clinical trial transparency