Global Data Management (Advanced)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

What You Will Be Doing:

• Manage and oversee data management activities across one or more clinical trials while ensuring alignment with study objectives.
• Ensure strict adherence to regulatory requirements, SOPs, work instructions, and established quality standards throughout the trial lifecycle.
• Maintain real-time inspection readiness and actively support both internal and regulatory audits.
• Build and sustain strong collaborative relationships with clinical trial teams, data management teams, and external partners.
• Act as a central point of contact to align expectations, timelines, and deliverables across all stakeholders.
• Participate in cross-functional clinical working groups to ensure seamless coordination and delivery of data management requirements.
• Gather and define requirements for eCRFs and other data collection tools, ensuring consistency in data quality, conventions, and dataset structure.
• Plan, track, and ensure timely delivery of key deliverables such as CRFs, data review plans, QC and oversight plans, database release plans, and final datasets.
• Ensure all data management documentation meets high standards of quality, clarity, accuracy, consistency, and regulatory compliance.
• Lead advanced-level activities by driving planning and execution, providing team leadership, sharing best practices, and delivering training sessions to support continuous improvement.

Your Profile:

• Bachelor’s degree in Life Sciences, Health Sciences, or a related discipline with 3+ years of clinical data management experience, including hands-on involvement in clinical trials.
• Strong expertise in clinical data management processes, systems, and regulatory requirements, with proven ability to operate in global, cross-functional, and multicultural environments.
• Demonstrated leadership, project management, and organizational skills, with experience managing vendors and driving complex deliverables to completion.
• Advanced proficiency in Microsoft Office, particularly in data analysis, with the ability to interpret clinical data and communicate clear, data-driven insights to stakeholders.
• Highly organized, detail-oriented, and proactive professional with a strong quality and compliance mindset, excellent communication skills, and a collaborative, solution-driven approach.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Are you a current ICON Employee? Please click here to apply