ICON plc is inviting applications for the position of Senior Global Regulatory Scientist to support global regulatory strategies, clinical development programmes, and regulatory submissions. The full-time opportunity is listed across multiple international locations, including Bangalore, India; Sydney, Australia; Auckland, New Zealand; Singapore; and Kuala Lumpur, Malaysia.
This senior-level role is suitable for experienced regulatory affairs professionals with a strong understanding of global clinical development regulations, scientific documentation, and health authority interactions. The selected candidate will contribute to regulatory strategy development, prepare and review complex regulatory documents, advise cross-functional teams, and mentor junior regulatory colleagues.
Candidates with experience in pharmaceutical, biotechnology, or contract research organization (CRO) environments may consider applying through ICON’s official careers portal.
ICON Senior Global Regulatory Scientist Recruitment 2026: Job Highlights
| Particulars | Details |
|---|---|
| Company | ICON plc |
| Job Title | Senior Global Regulatory Scientist |
| Job Requisition ID | JR158528 |
| Job Category | Regulatory Affairs / Regulatory Science |
| Job Type | Full-time |
| Listed Locations | Sydney, Auckland, Bangalore, Singapore, Kuala Lumpur, and other locations |
| Work Arrangement | Office or Home, depending on the listing |
| Qualification | Bachelor’s degree in a relevant scientific or healthcare-related discipline |
| Experience | Extensive relevant regulatory affairs or regulatory science experience |
| Travel Requirement | Approximately 10% |
| Salary | Not disclosed |
| Application Mode | Online |
About ICON plc
ICON plc is a global healthcare intelligence and clinical research organization that works with pharmaceutical, biotechnology, and other healthcare companies to support the development of medicines and treatments.
The organization provides clinical development and related research services, with teams working across regulatory, scientific, operational, and clinical functions.
Job Description: Senior Global Regulatory Scientist
The Senior Global Regulatory Scientist will provide scientific and regulatory expertise to support global clinical development programmes. The role involves creating regulatory strategies, interpreting changing regulatory requirements, preparing submission documents, and helping project teams make informed regulatory decisions.
The successful candidate will also work with sponsors, health authorities, and cross-functional teams while contributing to internal knowledge sharing and the development of junior colleagues.
Key Responsibilities
1. Global Regulatory Strategy
- Develop regulatory strategies for global clinical development programmes.
- Plan key health authority interactions and regulatory milestones.
- Provide regulatory input into clinical development plans and programme execution.
- Identify regulatory risks and contribute to suitable risk management approaches.
- Advise teams on labelling considerations and regulatory implications.
2. Regulatory Documentation and Submissions
- Prepare and review complex regulatory documents.
- Contribute to clinical trial applications, briefing books, and major regulatory submission components.
- Ensure regulatory positions are scientifically sound and supported by relevant evidence.
- Maintain high standards of accuracy, consistency, and documentation quality.
3. Regulatory Intelligence and Compliance
- Interpret evolving global regulations, guidelines, and regulatory precedents.
- Assess the implications of regulatory changes for clinical development programmes.
- Apply knowledge of requirements established by authorities such as the US Food and Drug Administration (FDA), European Medicines Agency (EMA), and International Council for Harmonisation (ICH).
- Consider regional regulatory requirements when developing global strategies.
4. Health Authority and Sponsor Interaction
- Represent regulatory functions during sponsor and health authority meetings.
- Communicate regulatory recommendations clearly and professionally.
- Support cross-functional discussions on regulatory issues and programme milestones.
- Help teams understand regulatory expectations and potential compliance risks.
5. Mentoring and Knowledge Sharing
- Provide guidance and mentoring to junior regulatory professionals.
- Contribute to internal regulatory best practices, templates, and knowledge-sharing activities.
- Support consistency and quality across regulatory projects.
Eligibility Criteria
Candidates should have a bachelor’s degree in a relevant scientific discipline or healthcare-related field.
The position requires substantial experience in regulatory affairs or regulatory science within the pharmaceutical, biotechnology, or CRO industry. Applicants should be able to work independently, handle complex regulatory matters, and guide colleagues when needed.
Required Skills
- Strong knowledge of global clinical development regulations.
- Understanding of FDA, EMA, ICH, and relevant regional requirements.
- Experience preparing or reviewing regulatory documentation.
- Familiarity with clinical trial applications and major regulatory submissions.
- Experience interacting with health authorities.
- Ability to lead cross-functional regulatory projects.
- Strong scientific writing and analytical skills.
- Excellent verbal and written communication.
- Critical thinking and attention to detail.
- Willingness to travel approximately 10% as required.
The job description does not specify a fixed minimum number of years of experience. However, the senior designation and requirement for extensive regulatory expertise indicate that the role is intended for experienced professionals.
Job Locations and Work Arrangement
The vacancy lists several international locations, including:
- Sydney, Australia
- Auckland, New Zealand
- Bangalore, India
- Singapore
- Kuala Lumpur, Malaysia
The listing also indicates that additional locations are available. Although the work arrangement is shown as Office or Home, the specific arrangement may vary by location and role. Candidates should confirm their preferred location and applicable work setup through the official application portal.
Employment is conditional on having the legal right to work in the country where the position is based.
Salary and Benefits
ICON has not disclosed a specific salary range for this position in the supplied job listing. Compensation may vary according to location, relevant experience, and employment terms.
Potential benefits may include:
- Competitive base salary and performance-related incentives.
- Medical, dental, and vision coverage where applicable.
- Retirement and pension plans.
- Life assurance and disability coverage.
- Employee assistance and wellbeing programmes.
- Structured learning, professional development, and career progression opportunities.
Benefits vary by country and employment arrangement.
How to Apply for ICON Senior Global Regulatory Scientist Jobs
Interested candidates can submit their applications through ICON’s official careers portal.
Before applying, prepare an updated resume highlighting regulatory strategy development, clinical development regulations, submission writing and review, health authority interactions, and cross-functional project leadership.
Select the appropriate location and review the role-specific requirements carefully. Applicants should also confirm local work authorization requirements and the applicable office or home-based arrangement.
Frequently Asked Questions (FAQs)
1. Which company is hiring for Senior Global Regulatory Scientist?
ICON plc is advertising the Senior Global Regulatory Scientist position.
2. What is the job requisition ID?
The requisition ID is JR158528.
3. Where are the jobs available?
The listing includes Bangalore, Sydney, Auckland, Singapore, Kuala Lumpur, and additional international locations.
4. What qualification is required?
A bachelor’s degree in a relevant scientific discipline or healthcare-related field is required.
5. How much experience is required?
The listing requires extensive experience in regulatory affairs or regulatory science but does not state a specific minimum number of years.
6. What are the main responsibilities?
The role includes global regulatory strategy, regulatory document preparation and review, clinical development support, regulatory intelligence, health authority interactions, and mentoring junior colleagues.
7. Is knowledge of FDA and EMA regulations important?
Yes. The candidate profile specifically highlights knowledge of global clinical development regulations, including FDA, EMA, ICH, and relevant regional requirements.
8. Is travel required?
Yes. The job description indicates approximately 10% travel, as required.
9. What is the salary for this position?
The salary is not disclosed in the supplied vacancy details.
10. How can candidates apply?
Candidates can apply through the official ICON careers link included in this article.
Disclaimer
This article is a rewritten summary of the job information provided in ICON’s recruitment listing. The availability of vacancies, location options, eligibility requirements, work arrangements, compensation, and benefits may change. Candidates should verify the latest details on the official application page before applying.