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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.

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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.

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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.

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Global Impact

Be part of a team that partners with leading pharmaceutical, biotechnology and medical device companies to improve patient lives worldwide.

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List #1

Roles in this area at ICON

Clinical Research Associate II

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

Sophie Clarke

Author

Sophie Clarke
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Senior Clinical Research Associate

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 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

Sophie Clarke

Author

Sophie Clarke
Read more Shortlist Save this role
Senior Informed Consent Specialist

Salary

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

Allen Hao

Author

Allen Hao
Allen Hao

Author

Allen Hao
Read more Shortlist Save this role
Clinical Site Associate

Salary

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

Daisy Park

Author

Daisy Park
Daisy Park

Author

Daisy Park
Read more Shortlist Save this role
Senior Director, Regulatory Affairs

Salary

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

Patrick Hale

Author

Patrick Hale
Read more Shortlist Save this role
Principal Auditor, Quality Assurance - CSV, AI & Risk Assessment

Salary

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

Maya Katsarska Read more Shortlist Save this role
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