Full Service
ICON Full Service
The Full Service model enables sponsors - pharmaceutical, biotechnology, and medical device companies - to focus on what they do best: developing innovative therapies and medical technologies that have the potential to transform lives.
By entrusting the complexities of clinical trials to ICON, sponsors gain a trusted partner that ensures every aspect of the trial process is executed efficiently, accurately, and in compliance with global regulations.
Shape the future of Clinical Research
Our Full Service division plays a pivotal role in advancing healthcare globally, combining innovation, expertise, and collaboration to execute some of the most complex and impactful clinical trials.
Join a team where your work has real-world impact, and your skills can help make a difference.
Why join ICON Full Service?
Career Growth
At ICON, your development is a priority. Gain exposure to diverse therapeutic areas, global operations, and advanced methodologies, all while building your career.
Work on Cutting-Edge Trials
From innovative study designs to advanced technologies like decentralised trials and AI powered analytics, ICON is leading the way in transforming clinical research.
Follow us on LinkedInGlobal Impact
Be part of a team that partners with leading pharmaceutical, biotechnology and medical device companies to improve patient lives worldwide.
View our jobsRoles in this area at ICON
Salary
Location
France, Paris
Department
Clinical Monitoring
Real World Solutions
Location
Paris
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II (CRA) to join our diverse and dynamic ICON Biotech team.Our biotech division of 8,000 people operates with a mindset aligned to small and mid-
Reference
JR152870
Expiry date
01/01/0001
Author
Sophie ClarkeAuthor
Sophie ClarkeSalary
Location
France, Paris
Department
Clinical Monitoring
Real World Solutions
Location
Paris
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic ICON Biotech team. Our biotech division of 8,000 people operates with a mindset aligned to small and
Reference
JR152871
Expiry date
01/01/0001
Author
Sophie ClarkeAuthor
Sophie ClarkeSalary
Location
China, Beijing
Location
Beijing
Chengdu
Shanghai
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
As a Senior Informed Consent Specialist at ICON, you will lead the development and oversight of informed consent strategies and documents for complex, global clinical studies. You will act as a subjec
Reference
JR150072
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
Korea, Seoul
Department
Clinical Monitoring
Location
Seoul
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Site Associate at ICON, you will support site management activities and ensure that clinical trials are conducted efficiently, compliantly, and to the highest quality standards.What You
Reference
JR155328
Expiry date
01/01/0001
Author
Daisy ParkAuthor
Daisy ParkSalary
Location
UK, Reading
Location
Reading
Blue Bell
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Drug / Device Regulatory Affairs
Job Type
Permanent
Description
As a Senior Director, Regulatory Affairs at ICON, you will provide strategic direction and management of Regulatory Affairs teams (up to 80 team members) and projects and contribute to the strategic d
Reference
JR152372
Expiry date
01/01/0001
Author
Patrick HaleAuthor
Patrick HaleSalary
Location
UK, Reading
Location
Dublin
Reading
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Quality Assurance
Job Type
Permanent
Description
What You Will Do:Audit Management & Execution:Plan, schedule, and conduct technology, data integrity, and process audits across internal functions and external vendorsDevelop risk-based audit plans, d
Reference
JR152125
Expiry date
01/01/0001
Author
Maya KatsarskaAuthor
Maya KatsarskaImpactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON