CRA II
Hi, I am Isabellaand I manage this role
Talent Acquisition Specialist
About the role
This vacancy has now expired. Please click here to view live vacancies.
Clinical Research Associate II
Location: Home based position, can be based anywhere in the U.S.
ICON plc is a world-leading healthcare intelligence and clinical research organization. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.
With our patients at the center 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:
* Independent, proactive work to set up and monitor studies, complete reports and maintain documentation
* Submitting protocol, consent documents for ethics/IRB approval, as well as preparing regulatory submissions
* Balancing sponsor generated queries
* Taking responsibility for study cost efficiency
* Preparation and review of study documentation and feasibility studies for new proposals
* Potential to assist in training and mentoring fellow CRAs
To be successful in the role, you will have:
* 18 months+ of monitoring experience in phase I-III trials as a CRA
* College degree in medicine, science, or equivalent
* Previous monitoring experience in medium-sized studies, including study start-up and close-out
* Knowledge of ICH-GCP guidelines and ability to review and evaluate medical data
* Excellent written and verbal communication
* Ability to work to tight deadlines
* Availability to travel least 60% of the time (international and domestic -fly and drive) and should possess a valid driving license
Benefits of Working in ICON:
Our success depends on the knowledge, capabilities and quality of our people. That's why we are committed to developing our employees in a continuous learning culture - one where we challenge you with engaging work and where every experience adds to your professional development.
At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.
ICON, including subsidiaries, 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.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
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
11/14/2025
Summary
Karina Espinoza's Journey at ICON Karina Espinoza's career in pharmacovigilance didn't begin with a grand plan. It started with a practical problem during her final year of a PhD in epidemiology, a
Teaser label
Our PeopleContent type
BlogsPublish date
11/13/2025
Summary
A Career Built on Patient Impact: Victoria DeVeaugh Geiss's Journey at ICON Victoria DeVeaugh Geiss has spent more than two decades in clinical research, and one thing has stayed constant throughout
Teaser label
IndustryContent type
BlogsPublish date
10/28/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
Similar jobs at ICON
Salary
Location
United States of America
Location
Multiple US Locations
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Support
Job Type
Permanent
Description
This role involves supporting the execution of clinical trials by managing administrative tasks and monitoring trial progress. The position is responsible for coordinating and tracking all study docum
Reference
JR139022
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
Japan, Tokyo
Location
Tokyo
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Corporate Support
Job Type
Permanent
Description
【職務内容】弊社のFSP部門(Functional Service Provider)における外部就労案件にてBusiness Operations Manager – Site Contracting(弊社タイトルManager, Contracts想定)として下記ご担当いただきます。※ご経験によっては、Business Operations Associate - Site Contracti
Reference
JR137772
Expiry date
01/01/0001
Author
Mai TakanashiAuthor
Mai TakanashiSalary
Location
US, Lenexa KCIB (PRA)
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Lenexa
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Medical & Scientific Affairs
Job Type
Temporary Employee
Description
We are currently seeking an Environmental, Health & Safety (EHS) Manager to join our diverse and dynamic team. As an EHS Manager at ICON, you will play a pivotal role in ensuring the safety and well-b
Reference
JR139106
Expiry date
01/01/0001
Author
Hanna PitcairnAuthor
Hanna PitcairnSalary
Location
Mexico, Mexico City
Department
Full Service - Medical Affairs & Pharmacovigilance
Location
Mexico City
Sofia
Warsaw
Remote Working
Office or Home
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Operations
Pharmacovigilance & Patient Safety
Job Type
Permanent
Description
What you will be doing: Conduct comprehensive reviews of clinical trial protocols, patient records, and medical documentation to ensure compliance with study protocols and regulatory requirements.Coll
Reference
JR138500
Expiry date
01/01/0001
Author
Florencia PistolesiAuthor
Florencia PistolesiSalary
Location
Brazil, Sao Paulo
Location
Sao Paulo
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
We are currently seeking a Clinical Research Associate to join our diverse and dynamic team at ICON Plc. As a key member of our research department, you will be responsible for overseeing and coordina
Reference
JR138529
Expiry date
01/01/0001
Author
Bruna DuarteAuthor
Bruna DuarteSalary
Location
Mexico, Mexico City
Location
Mexico City
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Regulatory Affairs
Job Type
Permanent
Description
Senior Regulatory TechnicianLocation: Mexico City only – Office based role (Hybrid)As a Senior Regulatory Technician you will work with the Clinical Trials Information System (CTIS), and will also
Reference
JR134308
Expiry date
01/01/0001
Author
Elizabeth DaviesAuthor
Elizabeth Davies