Description
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 Senior Global Regulatory Affairs Specialist at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.
Responsibilities:
- Developing global regulatory strategies for the successful submission and approval of clinical trial applications and marketing authorizations.
- Providing regulatory guidance and support to cross-functional teams throughout the drug development process.
- Ensuring compliance with global regulatory requirements and standards.
- Managing regulatory submissions and interactions with health authorities.
- Participating in regulatory intelligence activities to stay updated on changes in regulations and guidelines.
Your Profile:
- Bachelor's degree in a scientific discipline or related field.
- Minimum of 5 years of experience in regulatory affairs within the pharmaceutical or biotechnology industry.
- Strong understanding of global regulatory requirements and guidelines.
- Excellent communication and social skills.
- Ability to work independently and collaboratively in a fast-paced environment.
Rewards & 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