Job Description
Join ICON plc as a Clinical Trial Transparency Associate and play a key role in securing sensitive trial data. This position focuses on anonymizing documents while working with cross-functional teams in a global context.
In this position, you will oversee the anonymization of clinical trial documents in line with EU regulations and industry standards. You will collaborate with biostatistics, programming, and medical writing teams to ensure relevant datasets are processed accurately and timely. Your role will directly support clinical trial transparency initiatives at a global scale.
Key Responsibilities:
• Facilitate anonymization of datasets according to planned timelines
• Evaluate documents per EMA Policy 0070 guidelines
• Work with cross-functional teams for necessary document integration
• Implement anonymization plans reducing re-identification risks
• Ensure quality checks of anonymized documents are performed
...
In this position, you will oversee the anonymization of clinical trial documents in line with EU regulations and industry standards. You will collaborate with biostatistics, programming, and medical writing teams to ensure relevant datasets are processed accurately and timely. Your role will directly support clinical trial transparency initiatives at a global scale.
Key Responsibilities:
• Facilitate anonymization of datasets according to planned timelines
• Evaluate documents per EMA Policy 0070 guidelines
• Work with cross-functional teams for necessary document integration
• Implement anonymization plans reducing re-identification risks
• Ensure quality checks of anonymized documents are performed
...