Make an impact in clinical research with ICON plc as a Clinical Trial Anonymization Specialist. You'll handle the anonymization of crucial clinical trial documents and datasets remotely to ensure transparency.

At ICON, this role emphasizes collaboration with biostatistics and medical writing teams, driving the timely processing of anonymized documents. As part of your responsibilities, you will manage anonymization plans addressing regulatory requirements while reducing re-identification risks. Your expertise will play a vital role in supporting public disclosures under EU Clinical Trial Regulation and other pertinent policies.

Key Responsibilities:
• Manage anonymization timelines for datasets and documents
• Assess documents for public disclosure compliance
• Collaborate with teams to align documents for disclosure
• Develop strategies to mitigate re-identification risks
• Perform quality checks on anonymized documents