Anonymization Specialist for Clinical Trials at ICON
ICON • burlington, Canada
Role Description
Become an Anonymization Specialist with ICON plc, focusing on clinical trial document confidentiality. This role emphasizes collaboration with diverse teams to uphold transparency in clinical research.
As part of the Clinical Trial Transparency team, your responsibilities will include managing the anonymization of essential trial documents in compliance with regulatory frameworks. You will work closely with medical writers and statistic professionals to deliver anonymized datasets required for public transparency under EU directives. Your contributions will be crucial to maintaining the integrity of clinical trial reporting.
Key Responsibilities:
• Coordinate anonymization projects per regulatory timelines
• Assess clinical documents for public disclosure eligibility
• Collaborate with medical writing and programming teams
• Create plans for anonymization to limit re-identification risk
• Conduct quality assurance on redacted docu...
As part of the Clinical Trial Transparency team, your responsibilities will include managing the anonymization of essential trial documents in compliance with regulatory frameworks. You will work closely with medical writers and statistic professionals to deliver anonymized datasets required for public transparency under EU directives. Your contributions will be crucial to maintaining the integrity of clinical trial reporting.
Key Responsibilities:
• Coordinate anonymization projects per regulatory timelines
• Assess clinical documents for public disclosure eligibility
• Collaborate with medical writing and programming teams
• Create plans for anonymization to limit re-identification risk
• Conduct quality assurance on redacted docu...