What You Will Do:

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

Key responsibilities include:

• Developing and implementing regulatory strategies for global clinical trials.
• Providing expertise and guidance on regulatory requirements and compliance issues.
• Collaborating cross-functionally with teams to ensure regulatory objectives are met.
• Leading interactions with regulatory agencies and preparing submissions.
• Keeping abreast of regulatory updates and industry trends to inform strategy.

Your Profile:

You will have a strong background in regulatory affairs, with proven management experience and a commitment to quality delivery.

Required qualifications and experience:

• Bachelor's degree in a relevant scientific discipline or healthcare-related field
• Minimum of 5 years of experience in regulatory affairs within the pharmaceutical or biotech industry.
• Strong knowledge of global regulatory requirements and guidelines.
• Proven track record of successful regulatory submissions and interactions.
• Excellent communication, leadership, and problem-solving 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.

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