Salary
Location
US, Blue Bell (ICON)
Location
Frankfurt
Blue Bell
Remote Working
Remote
Job Categories
Medical Writing
Job Type
Permanent
Description
As a Principal Medical Writer at ICON, you will be responsible for leading the development of high-quality regulatory and clinical documents that effectively communicate scientific and medical informa
Reference
JR152737
Expiry date
01/01/0001
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Salary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Remote
Job Categories
Drug / Device Regulatory Affairs
Job Type
Permanent
Description
As a CMC Project Manager 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
Reference
JR151466
Expiry date
01/01/0001
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Salary
Location
US, Blue Bell (ICON)
Location
Burlington
Blue Bell
Remote Working
Remote
Job Categories
Medical Writing
Job Type
Permanent
Description
The Informed Consent Writer (ICW) is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language to help a candidate make an in
Reference
JR152535
Expiry date
01/01/0001
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Salary
Location
Quebec
Location
Quebec
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Sr. CRA at ICON, you will oversee and manage clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards.What You
Reference
JR152128
Expiry date
01/01/0001
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Salary
Location
United States of America
Location
Multiple US Locations
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activit
Reference
JR148352
Expiry date
01/01/0001
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Salary
Location
US, Blue Bell (ICON)
Location
Burlington
Blue Bell
Remote Working
Remote
Job Categories
Medical Writing
Job Type
Permanent
Description
The Informed Consent Writer (ICW) is responsible for preparing informed consent documents that disclose information about a clinical trial using health literate language to help a candidate make an in
Reference
JR149263
Expiry date
01/01/0001
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Salary
Location
Canada, Burlington
Location
Burlington
Remote Working
Remote
Job Categories
Medical Writing
Job Type
Permanent
Description
As a Clinical Trial Transparency Associate at ICON, you will be responsible for processing the anonymization of clinical trial documents and datasets required for public disclosure. The Anonymization
Reference
JR151336
Expiry date
01/01/0001
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Salary
Location
Boston, MA
Location
Ontario
New Brunswick
Nova Scotia
Quebec
Boston, MA
Remote Working
Remote
Job Categories
Drug Development
Job Type
Permanent
Description
The Senior Drug Development Project Manager oversees the high-level plans and progress of these teams, managing projects from pre-clinical stages through to commercialization. The DDPM is responsible
Reference
JR150504
Expiry date
01/01/0001
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Salary
Location
Canada
Location
Canada
Remote Working
Remote
Job Categories
Patient Recruitment
Job Type
Permanent
Description
As a Site Engagement Liaison at ICON, you will foster relationships with clinical trial sites, enhancing site engagement, and contribute to the advancement of innovative treatments and therapies.What
Reference
JR148491
Expiry date
01/01/0001
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Salary
Location
Canada
Location
Canada
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activit
Reference
JR145141
Expiry date
01/01/0001
Read more
Shortlist Save this role
Salary
Location
United States of America
Location
Multiple US Locations
Remote Working
Remote
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate (CRA) to join our diverse and dynamic team. As a CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activit
Reference
JR145140
Expiry date
01/01/0001
Read more
Shortlist Save this role
Teaser label
Our PeopleContent type
BlogsPublish date
06/10/2026
Summary
Why I Still Recommend the CTA Role After More Than 10 Years in Clinical Research Clinical Operations Manager Yordan Zahariev reflects on career growth, leadership and the opportunities a CTA role
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Teaser label
Our PeopleContent type
BlogsPublish date
06/04/2026
Summary
After more than 20 years at ICON, Carolina Boari has witnessed the organisation's growth across Latin America while building a successful career of her own. Today, as Executive Director of Clini
Teaser label
Our PeopleContent type
BlogsPublish date
05/26/2026
Summary
From Data Management to Leadership For Sajna Basant, a career in Biometrics has always been about more than data. “Data is not just numbers,” she explains. “It represents real people, their health