[Hiring] Global Labelling Lead @ICON plc

Role Description

As a Global labeling lead, you will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. This is a 12-month fixed term contract, fully homebased.

You will oversee regulatory affairs operations, balancing quality, timelines, and stakeholder expectations.

• Develop and implement regulatory labeling strategies for drug development projects.
• Ensure compliance with global regulatory requirements and standards related to labeling.
• Manage the creation, review, and approval of labeling documents, including package inserts, patient leaflets, and labels.
• Coordinate labeling activities with cross-functional teams, including regulatory affairs, clinical development, and quality assurance.
• Provide regulatory guidance and assist to internal teams and external clients on labeling-related issues.

Qualifications

• Bachelor's degree in a scientific discipline or related field.
• Minimum of 8 years of experience in regulatory affairs or labeling within the pharmaceutical or biotechnology industry.
• Strong understanding of global regulatory requirements and guidelines related to labeling.
• Excellent communication and interpersonal skills.
• Ability to work independently and collaboratively in a fast-paced environment.

Requirements

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

Benefits

• 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.