Clinical Data Manager

Overview

As a client-focused data lead in global trials, you drive high-quality, regulatory-compliant data delivery from start-up to database lock. You collaborate with sponsors and cross-functional teams to ensure data integrity and timely delivery within a mission-driven organisation. You shape data management strategies, mitigate risks, and pursue continuous improvement in a fast-paced setting. This role offers impact across global studies and a chance to advance clinical data delivery at ICON.

Pay / Benefits

• Competitive base salary
• Health, dental, and vision coverage
• Retirement and pension plans
• Life assurance and disability coverage
• Employee wellbeing resources
• Learning and development opportunities

Responsibilities

• Act as the primary data lead within cross-functional study teams and sponsor partnerships
• Drive study start-up activities including EDC build, system integrations, UAT, and key data management deliverables
• Oversee data review, reconciliation, vendor management, and database lock activities
• Ensure compliance with CDISC standards, ICH-GCP requirements, and regulatory expectations
• Identify and mitigate risks while driving continuous improvement and operational excellence

Key requirements

• 6+ years of Clinical Data Management or Clinical Data Science experience in a CRO or pharmaceutical environment
• Bachelor’s degree in Life Sciences, Health Sciences, or related discipline
• Proven experience leading studies across the full clinical trial lifecycle
• Experience as a primary Data Lead on complex studies and/or extensive hands-on data review and reconciliation across EDC, vendor, eCOA, IRT, and SAE data
• Strong vendor oversight and stakeholder management experience
• Hands-on experience with EDC systems, with Veeva EDC preferred
• Knowledge of CDISC standards, including SDTM
• Strong understanding of clinical trial processes, regulatory requirements, and ICH-GCP
• Excellent communication, problem-solving, and project leadership skills

• excellent communication
• problem-solving
• project leadership
• EDC systems expertise (Veeva EDC preferred)
• CDISC standards (SDTM)
• regulatory knowledge (ICH-GCP)

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