Senior CRA - Home or Office Based
About the role
This vacancy has now expired. Please click here to view live vacancies.
- Working independently and proactively to coordinate all necessary activities required to set up and monitor a study, completing accurate study status reports and maintaining study documentation
- Submission of protocol, consent documents for ethics/IRB approval and assist in preparing regulatory submissions as requested
- Participate in preparing and reviewing study documentation and feasibility studies for new proposals as required
- Managing sponsor generated queries efficiently and responsible for study cost effectiveness
- Dependent on level of experience you may assist in training and mentoring less experienced CRA's and/or manage CRA's working on international projects
- 18 months+ of monitoring experience in phase I-III trials as a CRA
- Availability to travel (plane or car) 60%
- Knowledge of ICG GCP guidelines and expertise to review and evaluate medical data
- Excellent communication and interpersonal skills, both written and verbal enabling you to deal with queries in a timely manner
- Ability to produce accurate work to tight deadlines within a pressurized environment
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. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
03/16/2026
Summary
Driving Study Start-Up: James Pereira's Journey at ICON James Pereira's career in clinical research has been shaped by a single driving question: how do we get studies started faster? From his earl
Teaser label
Inside ICONContent type
BlogsPublish date
03/15/2026
Summary
Who's Who In a Clinical Trial Team Clinical trials rely on large, cross functional teams working together across countries, time zones and specialisms. For those new to the industry, the number of
Teaser label
IndustryContent type
BlogsPublish date
02/16/2026
Summary
What Sponsors, CROs, and Sites Each Do Clinical research brings together many organisations, each with a specific role in delivering a clinical trial. For those new to the industry, the relationsh
Similar jobs at ICON
Salary
Location
Ireland, Dublin
Department
Full Service - Commercial Solutions
Location
Dublin
Reading
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Proposals
Job Type
Permanent
Description
We are currently seeking a Proposals Development Associate II to join our diverse and dynamic team. As a Proposals Development Associate II at ICON, you will play a pivotal role in the development of
Reference
JR147122
Expiry date
01/01/0001
Author
Katty Barreto MaiaAuthor
Katty Barreto MaiaSalary
Location
China, Beijing
Location
Beijing
Chengdu
Guangzhou
Shanghai
Wuhan
Remote Working
Hybrid
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Permanent
Description
Job Advert PostingWe are currently seeking a Site Specialist I/II/Sr to join our diverse and dynamic team. As a Site Specialist I/II/Sr at ICON, you will play a pivotal role in designing and analyzing
Reference
JR141473
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
We are currently seeking a Clinical Trial Administrator to join our diverse and dynamic team. As a Clinical Trial Administrator at ICON, you will play a pivotal role in assisting with the design and a
Reference
JR145795
Expiry date
01/01/0001
Author
Michal CzyrekAuthor
Michal CzyrekSalary
Location
China, Changsha
Department
Clinical Monitoring
Location
Guangzhou
Shanghai
Wuhan
Changsha
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate II to join our diverse and dynamic team. As a Clinical Research Associate II at ICON, you will play a pivotal role in designing and analyzing cli
Reference
JR142961
Expiry date
01/01/0001
Author
Allen HaoAuthor
Allen HaoSalary
Location
UK, Livingston
Location
Paris
Dublin
Milan
Madrid
Mechelen
Assen
Livingston
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Pharmacokenetics
Job Type
Permanent
Description
We are seeking an experienced Clinical Pharmacology professional to support protocol development and pharmacokinetic/pharmacodynamic (PK/PD) analysis across Phase I–IV clinical trials as Senior PK Sci
Reference
JR146673
Expiry date
01/01/0001
Author
Niki ScottoAuthor
Niki ScottoSalary
Location
Poland, Warsaw
Location
Warsaw
Madrid
Remote Working
Remote
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
JR146212
Expiry date
01/01/0001
Author
Dagmara DrozdowskaAuthor
Dagmara Drozdowska