Shape the Future of Healthcare in Regulatory Affairs
Regulatory Affairs Roles
- Regulatory Affairs Associate
- Senior Regulatory Affairs Specialist
- Manager, Regulatory Submissions
- Director, Regulatory Strategy
Why ICON?
- Contribute to groundbreaking therapies that transform lives
- Collaborate with international teams to ensure regulatory compliance across diverse markets
- Access to continuous learning and opportunities to advance your career
Salary
Location
Mexico, Mexico City
Department
Drug Safety & Pharmacovigilence
Location
Mexico City
Remote Working
Office Based
Job Categories
Pharmacovigilance & Patient Safety
Job Type
Permanent
Description
What You Will Be Doing:Assist in organizing and coordinating medical team meetings and activities.Manage and maintain medical documentation and records.Coordinate communication and information flow be
Reference
JR130842
Expiry date
01/01/0001
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Salary
Location
Poland, Warsaw
Department
Drug Safety & Pharmacovigilence
Location
Warsaw
Remote Working
Office Based
Job Categories
Pharmacovigilance & Patient Safety
Job Type
Permanent
Description
We are currently seeking a Medical Admin Assistant I to join our diverse and dynamic team. As a Medical Admin Assistant I at ICON, you will play a pivotal role in providing essential administrative sc
Reference
JR130941
Expiry date
01/01/0001
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Salary
Location
India, Chennai
Department
Drug Safety & Pharmacovigilence
Location
Chennai
Remote Working
Office Based
Job Categories
Physician
Job Type
Permanent
Description
Job Advert PostingAt ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’
Reference
JR130468
Expiry date
01/01/0001
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Salary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Office Based
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Pharmacovigilance Assistant I/II/Senior to join our diverse and dynamic team based in our Warsaw offices. As part of the Pharmacovigilance team at ICON you will play a vital
Reference
JR128528
Expiry date
01/01/0001
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Salary
Location
Poland, Warsaw
Department
Clinical Trial Management
Location
Warsaw
Remote Working
Office Based
Job Categories
Regulatory Document Management
Job Type
Permanent
Description
We are currently seeking a TMF Specialist I to join our diverse and dynamic team. As a TMF Specialist I at ICON, you will play a vital role in becoming familiar with Trial Master File (TMF) documentat
Reference
JR131984
Expiry date
01/01/0001
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Salary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Mexico City
Remote Working
Home or Office
Job Categories
Drug / Device Regulatory Affairs
Job Type
Temporary Employee
Description
At ICON, it’s our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients’ lives. Our ‘Own I
Reference
JR131937
Expiry date
01/01/0001
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Salary
Location
Brazil
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Brazil
Remote Working
Home-Based
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotech
Reference
2025-119840
Expiry date
01/01/0001
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Salary
Location
Mexico
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Mexico
Remote Working
Home-Based
Job Categories
Drug Safety
Job Type
Permanent
Description
We are currently seeking a Graduate Pharmacovigilance Associate to join our diverse and dynamic team. As a Graduate Pharmacovigilance Associate at ICON, you will play an essential role in supporting t
Reference
2025-120328
Expiry date
01/01/0001
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Salary
Location
Europe
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Any EMEA Location
Remote Working
Home-Based
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
Regional CTA submission manager (EU CTR) - Homebased in UK or Europe An exciting new role with ICON within our regulatory team working on high profile Pharma projects with a client with which ICON sha
Reference
2025-120090
Expiry date
01/01/0001
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Salary
Location
Czech Republic, Slovakia
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Czech Republic
Slovakia
Remote Working
Home-Based
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
Regional CTA submission manager (EU CTR) - Homebased in Czechia/Slovakia ONLY An exciting new role with ICON within our regulatory team working on high profile Pharma projects with a client with which
Reference
2025-120091
Expiry date
01/01/0001
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Salary
Location
Europe
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
Any EMEA Location
Remote Working
Home-Based
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
As a Manager, Regulatory CMC (lifecycle management) you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. We are seeking 2 ro
Reference
2025-120133
Expiry date
01/01/0001
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Teaser label
IndustryContent type
BlogsPublish date
01/18/2024
Summary
Introduction to Regulatory Affairs in Clinical Research Regulatory affairs play a pivotal role in ensuring the safety, efficacy, and quality of pharmaceutical products and medical devices. In the
Teaser label
Inside ICONContent type
BlogsPublish date
02/17/2023
Summary
Clinical research is the backbone of the medical industry. Without it, it would be impossible for drugs and medical treatments to prove compliance and become approved for market sale. Drug safety
Teaser label
Inside ICONContent type
BlogsPublish date
09/29/2022
Summary
A Drug Safety Associate is responsible for assessing the safety of pharmaceuticals drugs once they’re on the market. Using standardised guidelines, they determine whether the medication causes any adv