Inspiring Positive Change in Clinical Research
We are the world’s leading CRO powered by Healthcare Intelligence, with a singular focus on improving the lives of patients by accelerating the development of our customer’s drugs and devices. As industry leaders, we own the responsibility to enhance the way clinical research works.
Empowered by our Healthcare Intelligence capabilities and the excellence of our people, we are breaking the boundaries of traditional thinking to find new ways to make it easier for patients to participate in clinical research and help our customers to bring medicines to market faster and at lower cost.
Roles & Responsibilities of Clinical Monitors
Compliance & Quality
Clinical Monitors play a pivotal role in maintaining integrity & accuracy of clinical trials.
- Verify that clinical trials are conducted in compliance with protocols, Good Clinical Practice (GCP), and regulatory requirements.
- Review site documents and ensure proper documentation of all study-related activities.
- Monitor patient safety by ensuring accurate and complete reporting of adverse events.
Site Management
As the primary point of contact between the trial sponsor & study sites, Clinical Monitors foster strong relationships to ensure trial success.
- Conduct site initiation, routine monitoring, and close-out visits.
- Train site staff on trial protocols and compliance requirements.
- Provide ongoing support and guidance to resolve site-related challenges.
Data Oversight
Clinical Monitors ensure the integrity of trial data through meticulous review and proactive issue management.
- Verify data accuracy by cross-checking source documents with electronic data capture (EDC) systems.
- Identify discrepancies, raise queries, and collaborate with site staff to resolve them.
- Document all findings in monitoring reports to maintain a clear audit trail.
Salary
Location
China, Beijing
Location
Beijing
Tianjin
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do
Reference
JR153866
Expiry date
01/01/0001
![Huixin "Stella" Song](https://attraxcdnprod1-freshed3dgayb7c3.z01.azurefd.net/1481126/e40ce6f4-d08e-41da-9b68-65e34e789e42/2026.7.1.18661/img/vxM7yWMXKE-o6Qjalvh9Zw/0/Huixin "Stella" Song)
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Salary
Location
China, Shanghai
Location
Shanghai
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. What You Will Do
Reference
JR150396
Expiry date
01/01/0001
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Salary
Location
Italy, Milan
Location
Milan
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will con
Reference
JR154616
Expiry date
01/01/0001
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Salary
Location
China, Shanghai
Location
Shanghai
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina
Reference
JR146637
Expiry date
01/01/0001
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Salary
Location
Taiwan, Taipei
Location
Taipei
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do:You will
Reference
JR155287
Expiry date
01/01/0001
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Salary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. This position is
Reference
JR155397
Expiry date
01/01/0001
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Salary
Location
France, Paris
Location
Paris
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical
Reference
JR145797
Expiry date
01/01/0001
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Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.What You Will Do:You will
Reference
JR155215
Expiry date
01/01/0001
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Salary
Location
Greece, Athens
Location
Athens
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do:You will
Reference
JR155442
Expiry date
01/01/0001
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Salary
Location
China, Shanghai
Location
Shanghai
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:
Reference
JR155226
Expiry date
01/01/0001
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Salary
Location
China, Shanghai
Location
Shanghai
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards.What You Will Do:
Reference
JR155227
Expiry date
01/01/0001
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Salary
Location
China, Beijing
Location
Beijing
Remote Working
Remote or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a CRA II at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. What You Will Do:You will
Reference
JR155225
Expiry date
01/01/0001
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Teaser label
A Day In The LifeContent type
BlogsPublish date
04/05/2023
Summary
Senior Clinical Research Associate Suzaita Hipolito talks about the satisfaction gained from working in Clinical Research. “What would it look like to wake up every day feeling happy and fulfil
