Clinical Trial Pack Design Specialist - Label Creator

Clinical Trial Pack Design Specialist – Label Creator

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.

As a Senior Clinical Supply Specialist at ICON, you will oversee the management and distribution of clinical trial supplies, ensuring that all materials are delivered efficiently and in compliance with regulatory requirements.

What You Will Do

You will take ownership of clinical supplies and logistics deliverables, applying your expertise to complex challenges.

Key responsibilities include:

• Work within a global team. Create master label content according to existing processes and procedures, designing Clinical Trial labels.
• Perform quality critical checks of label content produced in various languages to required timelines
• Perform quality critical checks of externally produced vendor label proofs prior to receipt by GSK
• Creation of label documentation, required for in-country regulatory submissions, in a timely manner.
• Highlight label quality issues
• Work with external vendors (translation service provider, component suppliers etc)
• Participate in GPM team meetings. [GPM stands for Global Pack Management]
• Liaise with other groups within Clinical Manufacturing & Supply Chain

Your Profile

You will have a strong foundation in clinical supplies and logistics, with the experience to work independently and guide others.

Required qualifications and experience:

• Bachelor's degree in supply chain management, logistics, life sciences, or a related discipline
• Significant experience in managing clinical supply, with a strong understanding of clinical trial requirements and regulatory standards.
• Experience within cGMP environment
• Proficiency in supply chain management tools and data analysis, with experience in using software for tracking and reporting.
• Strong communication, interpersonal, and stakeholder management skills, with the ability to build effective partnerships and drive successful outcomes in a fast-paced environment.

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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 .