Responsibilities

• Provide expert-level functional knowledge in at least one standards domain, contributing to the development of standards content for both internal projects and sponsor-facing initiatives.
• Develop, implement, and maintain ICON standards libraries in compliance with CDISC, sponsor, and regulatory requirements.
• Act as a subject matter expert to guide standards implementation and ensure compliance across clinical data management activities.
• Apply a deep understanding of business challenges to recommend and drive best practices, enhancing processes, products, and services.
• Collaborate cross-functionally to define data collection strategies and standards for clinical trials.
• Participate in standards governance activities, influencing decision-making and providing expert insights.

Requirements

• Master's degree in a relevant field or equivalent experience.
• Extensive experience in clinical data management and familiarity with data standards such as CDISC.
• Strong analytical skills with the ability to interpret complex data and provide actionable insights.
• Excellent communication and interpersonal skills to collaborate effectively with diverse teams.
• Proven track record of leading cross-functional projects and influencing stakeholders at all levels.
• Detail-oriented with a commitment to maintaining high standards of quality and compliance.

Benefits

• Competitive salary and performance-based bonuses.
• Comprehensive health and wellness benefits.
• Opportunities for professional development and career advancement.
• A supportive and inclusive work environment that values diversity.
• Flexible working arrangements to promote work-life balance.
• Access to innovative tools and technologies to enhance your work experience.