Clinical Trial Transparency Associate at ICON

Enhance public clinical trial disclosure efforts as a Clinical Trial Transparency Associate with ICON Strategic Solutions. Oversee anonymization processes to support EU regulations and health authority requirements.

In this role, you will work as a Clinical Trial Transparency Associate specializing in anonymization  will process clinical trial documents and datasets while collaborating with biostatistics and medical writing teams. With a minimum of three years in health sciences or related industries, you will demonstrate strong analytical skills and thorough knowledge of global regulatory guidelines.

Key Responsibilities:

• Manage and facilitate anonymization against planned timelines

• Assess documents for public disclosure compliance

• Collaborate with biostatistics and writing teams

• Develop anonymization plans to mitigate re-identification risk

• Ensure accurate redaction of clinical trial documents

Requirements:

• Bachelor's degree in a scientific or technical field

• Minimum 3 years' related work experience

• Strong knowledge of clinical trial disclosure guidelines

• Proficient in Excel and document management systems

• Excellent communication and project management skills

Leverage your expertise in clinical trial transparency to support ICON's mission of improving patient outcomes.
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