Drug Safety Associate
About the role
This vacancy has now expired. Please click here to view live vacancies.
- Your primary responsibility will be validating and quality checking safety database fields on assigned projects.
- You will also provide input for and review relevant safety tracking systems for accuracy/quality and perform safety review of clinical data (case report forms) and patient labs.
- You will also be responsible for documenting and processing serious adverse event cases within ICON, regulatory authorities and sponsor regulations and timeframes.
- With a science degree, pharmacy or nursing background or equivalent, you will have previous experience in a drug safety environment together with strong knowledge of medical terminology.
- You will have knowledge of drug safety databases, preferably ARGUS.
- You will have the ability to produce high quality work, with meticulous attention to detail.
- You will be fluent in verbal and written English, with excellent communication skills.
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
08/25/2025
Summary
Careers in Pharmacovigilance Pharmacovigilance, also known as drug safety, is one of the most important pillars of modern medicine. It ensures that once a medicine is developed, tested, and appro
.png)
Teaser label
Our PeopleContent type
BlogsPublish date
08/14/2025
Summary
A Leader’s Journey: Karen Hahn on Growth, Culture and the Future of ICON Mexico Karen Hahn’s career at ICON has unfolded over more than 15 years, shaped not by a rigid plan, but by openness to ch
.png)
Teaser label
Inside ICONContent type
BlogsPublish date
08/07/2025
Summary
Building a Career at ICON: A Conversation with Susie McEvoy, Senior VP of HR At ICON, career journeys are rarely linear – and Susie McEvoy’s story is a powerful example of that. From joining as a
Similar jobs at ICON
Salary
Location
United States
Department
Clinical Operations Roles
Location
United States
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
As a Senior Clinical Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-122031
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
Brazil
Department
Clinical Trial Management
Location
Brazil
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Manager to join our diverse and dynamic team at ICON Plc. In this critical role, you will be responsible for overseeing the planning, execution, and successfu
Reference
2025-121983
Expiry date
01/01/0001
Author
Simone ChanAuthor
Simone ChanSalary
Location
Johannesburg
Department
Clinical Monitoring
Location
Johannesburg
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Senior CRA Oncology/Hematology - Johannesburg (Home based) As a Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligen
Reference
2025-121827
Expiry date
01/01/0001
Author
Shelley BallAuthor
Shelley BallSalary
Location
Taipei
Department
Clinical Monitoring
Location
Taipei
Remote Working
Office Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
Clinical Research Associate (Oncology Team) Working Model: Taiwan Client Office based (Flexible WFH) As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clini
Reference
2025-122045
Expiry date
01/01/0001
Author
Sandy TangAuthor
Sandy TangSalary
Location
Taipei
Department
Clinical Monitoring
Location
Taipei
Remote Working
Office Based
Business Area
ICON Strategic Solutions
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 organisation, powered by healthcare intelligence.Working location: Client offic
Reference
2025-121486
Expiry date
01/01/0001
Author
Sandy TangAuthor
Sandy TangSalary
Location
Poland
Department
Clinical Operations Roles
Location
Poland
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
Clinical Trial Assistant assists in the coordination and administration of the study activities from the start up to execution and close out, and within the Local Study Team (LST) to ensure quality an
Reference
2025-121706
Expiry date
01/01/0001
Author
Michal CzyrekAuthor
Michal Czyrek