What You Will Do:

Technologies Role:

• Serve as business owner and subject matter expert for the N-SIDE forecasting suite and related clinical supply planning technologies.

• Lead study builds, forecasting models, system configuration, and IRT integrations for new clinical studies.

• Develop and deliver user training, documentation, and ongoing system support.

• Partner with Clinical Supply planners to develop and optimize forecasting models and planning assumptions.

• Collaborate with Clinical Operations, Technical Operations, IMSC, and IT to implement and enhance clinical supply technologies and system integrations.

• Coordinate user requirements, testing, issue resolution, and implementation activities with internal stakeholders and technology vendors.

• Identify opportunities to improve forecasting processes, reporting, automation, and data quality.

• Support system governance, documentation, change management, and continuous process improvement.

For Assigned Programs (as needed)

• Represent Clinical Supply Chain on cross-functional study teams.

• Develop and maintain clinical supply forecasts, inventory plans, and supply strategies for assigned studies.

• Coordinate supply planning activities with Clinical Operations, IMSC, Technical Operations, Procurement, and external vendors.

• Manage co-medication sourcing, budgets, and inventory, as applicable.

• Support IRT strategy, user acceptance testing, and ongoing supply management.

• Lead clinical supply meetings and communicate supply risks, mitigation plans, and study status to stakeholders.

• Monitor inventory, expiry, study timelines, and key supply metrics to ensure uninterrupted clinical supply.

• Maintain study documentation and escalate significant supply risks or timeline concerns as appropriate.

• Facilitate discussions and decisions on label and packaging design, as needed.

For Department:

• Develop and maintain SOPs, work instructions, and training materials.

• Lead or support departmental process improvement and technology initiatives.

• Share best practices and promote cross-functional collaboration.

• Represent Global Clinical Supply Chain on internal and external initiatives, as appropriate.

Your Profile:

• Bachelor's degree in a scientific, engineering, supply chain, business, or related discipline.

• 4+ years of experience in clinical supply chain or pharmaceutical development.

• 2+ years of hands-on experience with clinical supply forecasting, inventory planning, or simulation tools.

• Experience with N-SIDE, IRT systems, or comparable clinical supply technologies.

• Experience supporting system implementations, integrations, user acceptance testing, and change management.

• Understanding of global clinical trials, clinical supply processes, cGMP, and GCP.

• Proficiency with Microsoft Excel and data analysis.

• Strong project management, organizational, analytical, and problem-solving skills.

• Excellent written and verbal communication skills.

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 to read more about the benefits ICON offers.