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
Chicago, United States
Department
Clinical Monitoring
Location
Chicago
United States
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
Reference
2025-120826
Expiry date
01/01/0001
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Salary
Location
New York, United States
Department
Clinical Monitoring
Location
New York
United States
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
Reference
2025-120825
Expiry date
01/01/0001
Read more
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Salary
Location
Chicago
Department
Clinical Monitoring
Location
Chicago
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119487
Expiry date
01/01/0001
Read more
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Salary
Location
United States
Department
Clinical Monitoring
Location
United States
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organization, powered by healthcare intelligence.
Reference
2025-119052
Expiry date
01/01/0001
Read more
Shortlist Save this role
Salary
Location
United States
Department
Clinical Monitoring
Location
United States
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120934
Expiry date
01/01/0001
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Salary
Location
Argentina
Department
Clinical Monitoring
Location
Argentina
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Study Start-Up CRA (SSU CRA) will be responsible of creating and endorsing submission packages related to the country or site, following ICH, GCP, and all relevant regulations, laws, guidelines,
Reference
2025-120829
Expiry date
01/01/0001
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Salary
Location
Canada
Department
Clinical Monitoring
Location
Canada
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
ICON is looking for a CRA Line Manager in Canada to support one of our FSP programs. The role of the Line Manager is to line manage CRAs and/or CTAs effectively, ensuring high performance, quality and
Reference
2025-120947
Expiry date
01/01/0001
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Salary
Location
Boston, United States, Providence, Portland
Department
Clinical Monitoring
Location
Boston
Portland
Providence
United States
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Senior CRA (ONC) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119214
Expiry date
01/01/0001
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Salary
Location
France
Department
Clinical Monitoring
Location
France
Remote Working
Home-Based
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us
Reference
2025-117864
Expiry date
01/01/0001
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Salary
Location
Turkey, Ankara
Department
Clinical Monitoring
Location
Ankara
Remote Working
Home or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in desig
Reference
JR131841
Expiry date
01/01/0001
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Salary
Location
Italy, Milan
Department
Clinical Monitoring
Location
Milan
Remote Working
Home or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate at ICON, you’ll work within a large-scale, fast-paced environment alongside a close-knit team of highly qualified CRAs to identify, select, initiate and close-out inve
Reference
JR132158
Expiry date
01/01/0001
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Salary
Location
China, Guangzhou
Location
Guangzhou
Shanghai
Remote Working
Home or Office
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II Specialist to join our diverse and dynamic team. As a Clinical Research Associate II Specialist at ICON, you will play a pivotal role in desig
Reference
JR129978
Expiry date
01/01/0001
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Teaser label
Our PeopleContent type
BlogsPublish date
08/29/2023
Summary
To excel as a Clinical Research Associate (CRA) in a Clinical Research Organization (CRO), you need a combination of education, skills, and the right mindset. Brazil-based CRA II Debora shares her
Teaser label
Our PeopleContent type
BlogsPublish date
05/23/2023
Summary
How to progress as a Clinical Research AssociateTo thrive as a Clinical Research Associate (CRA), it is imperative to cultivate a multifaceted skill set and demonstrate unwavering commitment to excell
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 fulfilled?
