CRA - location : Paris or Lyon or Toulouse
About the role
This vacancy has now expired. Please click here to view live vacancies.
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, biotechnology, medical device and government and public health organisations.
With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.
Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.
The Role
At ICON Biotech Solutions, our culture is centered around support, growth and development and a drive to innovate.
ICON Biotech Solutions offers our CRA's in France the opportunity to gain a wide range of therapeutic experience and to work within an open and transparent environment with a focus on offering a flexible and adaptable mindset and approach to make our clients needs.
As a CRA you will be part of a multi-national team of Clinical Trials professionals who have access to excellent working tools and work within a supportive and collaborative environment.
Our Biotech Solutions Clinical Delivery team is world class and we are proud to offer huge opportunity for career growth and development through our internal training programs and pre established promotion pathways, ongoing mentoring and employee reward and recognition.
Clinical Research Associates are ultimately responsible for the successful management of investigator sites throughout the trial lifecycle. You will have the opportunity to work on a range of therapeutic areas and supported on your ICON journey by both a dedicated functional manager and also the cutting edge and user friendly technology that we have here at ICON.
Key responsibilities include:
Full ownership of investigator sites for assigned studies with responsibility for the successful management of the site right through to close-out.
Planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan.
Developing effective relationships with investigator site staff to ensure that key clinical metrics are met.
Preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues.
Ensuring integrity of clinical data through an ability to sufficiently maintain site tracking records and work diligently to relevant guidelines
You will be operating as a key part of a global study team and plays a fundamental role in our clients' drug development processes.
The Requirements
Here at ICON we want our employees to succeed and ensure that they are set up for this success through constant training, development and support. To enable success in this position you will have:
Prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment.
A working knowledge of ICH-GCP guidelines and local and international regulatory requirements is essential.
You will be educated to degree level, have equivalent experience or be a licensed healthcare professional.
ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
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
05/29/2025
Summary
Blood Cancer Day Blood Cancer Day is a powerful reminder of the millions of individuals and families whose lives are affected by hematological malignancies every year. These diseases are complex,
.png)
Teaser label
IndustryContent type
BlogsPublish date
05/22/2025
Summary
World Schizophrenia Awareness Day 2025 Every year on 24 May, World Schizophrenia Awareness Day offers a vital opportunity to raise awareness, dismantle stigma, and celebrate the strength of individ
.png)
Teaser label
Inside ICONContent type
BlogsPublish date
05/08/2025
Summary
Standing Strong on Ovarian Cancer Day: ICON's Commitment to Advancing Care Ovarian cancer remains one of the most challenging gynaecologic malignancies, both in terms of detection and treatmen
Similar jobs at ICON
Salary
Location
Turkey, Ankara
Location
Ankara
Remote Working
Hybrid: Office/Remote
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Data Management
Job Type
Permanent
Description
We are currently seeking a Tech Reporting Specialist II to join our diverse and dynamic team. As a Tech Reporting Specialist II at ICON, you will play a crucial role in enhancing our reporting capabil
Reference
JR130613
Expiry date
01/01/0001
Author
Tereza SvobodovaAuthor
Tereza SvobodovaSalary
Location
US, Blue Bell (ICON)
Location
Blue Bell
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Research In-Home Services
Job Type
Permanent
Description
Supervisor, Home Health Supplies (Floor Supervisor)Onsite - Blue Bell, PAWe are currently seeking a Supervisor, Home Health Supplies (Floor Supervisor) to join our diverse and dynamic team. As a Super
Reference
JR129631
Expiry date
01/01/0001
Author
Sasha BrownAuthor
Sasha BrownSalary
Location
US, Salt Lake City (PRA)
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Salt Lake City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Study Start Up
Job Type
Temporary Employee
Description
We are currently seeking a Clinical Trial Recruitment Representative to join our diverse and dynamic team at ICON at our Salt Lake City UT site. Location: On-Site Salt Lake City UTJob Type: PRN/As Nee
Reference
JR129814
Expiry date
01/01/0001
Author
Stephanie CurranAuthor
Stephanie CurranSalary
Location
Czech Republic, Prague
Department
Clinical Monitoring
Location
Prague
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Intern
Job Type
Intern
Description
We are currently seeking an Intern to join our diverse and dynamic team. As an Intern at ICON, you will have the opportunity to gain hands-on experience in a professional environment, supporting vario
Reference
JR131143
Expiry date
01/01/0001
Author
Lauren PritchettAuthor
Lauren PritchettSalary
Location
US, Blue Bell (ICON)
Department
Full Service - Development & Commercialisation Solutions
Full Service - Global Business Services
Location
New York
Blue Bell
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Project/ Program Management
Job Type
Permanent
Description
Program Manager, Labs – Blue Bell PA, Farmingdale NY- Hybrid. Assist the team of PMs in issue resolution / escalation during the lifetime of all trials • Understand your Project Managers’ performa
Reference
JR130137
Expiry date
01/01/0001
Author
Frank LampartAuthor
Frank LampartSalary
Location
United States
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
United States
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Other
Job Type
Permanent
Description
As a Surgical Science Liaison (Neurosurgery) – Part-time/Contract, you will join the world’s largest and most comprehensive clinical research organization, driven by healthcare intelligence.
Reference
2025-119361
Expiry date
01/01/0001