Clinical Research Coordinator
About the role
This vacancy has now expired. Please click here to view live vacancies.
Do you have experience coordinating and ensuring execution of
all clinical study protocol activities?
ICON plc is looking for a Clinical Research Coordinator to
join our team in San Antonio, TX! We are named by Forbes as one of the best
employers for the third year in a row! We are a top five clinical research
organization with stability, solid earnings and growth potential with 13,500
employees in forty countries globally.
The Clinical Research Coordinator (CRC) will coordinate and
ensure execution of all clinical study protocol activities within Good Clinical
Practice (GCP) and the Food and Drug Administration (FDA) regulations and
requirements, Sponsor expectations and ICON Early Phase Standard Operating
Procedures (SOPs). The CRC will work with study Principle/Sub Investigators
(Sub-PI), Study Managers and Clinical Manager for project scheduling and
design. The CRC should have a basic understanding of research methods and
various research study design to identify and ensure successful clinical studies
preparation, site initiation, monitoring and closeout
visits.
Benefits of working at ICON:
In addition to partnering with the top pharmaceutical and
biotech companies in the world we offer a strong benefits package that includes
a comprehensive health plan, retirement plans, competitive pay, bonus plans,
vacation, and other incentives.
To succeed you will need:
We are seeking candidates with a Bachelor’s degree in a
related field OR Certified/Registered Medical Assistant (CMA/RMA), Licensed
Vocational Nurse (LVN), Registered Nurse (RN), Emergency Medical Technician
(EMT). Certified Clinical Research Coordinator (CCRC)
preferred.
To be successful you will be expected to have at least two
years medical experience, previous research experience and be proficient with
Microsoft Office.
What’s Next?
Following your application you will be contacted by one of our dedicated recruiters and if successful we will be able to provide you with more details about this opportunity.
ICON is an equal opportunity employer - Minorities/Females/Disabled/Veterans and committed to providing a workplace free of any discrimination or harassment.
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
IndustryContent type
BlogsPublish date
04/03/2026
Summary
Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re
Teaser label
Our PeopleContent type
BlogsPublish date
03/26/2026
Summary
Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February
Teaser label
Our PeopleContent type
BlogsPublish date
03/24/2026
Summary
Career paths are rarely straightforward, especially in the fast moving world of clinical research. For many professionals, gaining experience across organisations can provide valuable perspectiv
Similar jobs at ICON
Salary
Location
Bulgaria, Sofia
Location
Sofia
Warsaw
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Safety Scientist
Job Type
Permanent
Description
We are currently seeking a Principal Safety Scientist to join our diverse and dynamic team. As a Principal Safety Scientist at ICON, you will be responsible for leading safety assessments and pharmaco
Reference
JR148065
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
Poland, Warsaw
Location
Warsaw
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Contracts Administration
Job Type
Permanent
Description
We are currently seeking a Senior Site Contracts Negotiator to join our diverse and dynamic team. As a Senior Site Contracts Negotiator at ICON, you will lead the negotiation of clinical trial agreeme
Reference
JR145278
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
Czech Republic, Prague
Location
Prague
Bratislava
Remote Working
Remote or Office
Business Area
ICON Full Service & Corporate Support
Job Categories
Contracts Administration
Job Type
Permanent
Description
Job Advert posting missing
Reference
JR144800
Expiry date
01/01/0001
Author
Magda KozuszekAuthor
Magda KozuszekSalary
Location
France, Lyon
Location
Paris
Lyon
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
We are currently seeking a Study Start Up Associate I to join our diverse and dynamic team. As a Study Start Up Associate I at ICON, you will play a pivotal role in facilitating the initiation of clin
Reference
JR148079
Expiry date
01/01/0001
Author
Elisabeth TrivicAuthor
Elisabeth TrivicSalary
Location
Miami, FL
Location
Miami, FL
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
What You Will Be Doing:Serve as the primary point of contact between investigational sites and the sponsorConduct all types of site visits, including selection, initiation, routine monitoring, and clo
Reference
JR148307
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica HawkinsSalary
Location
US, Lenexa KCI (PRA)
Department
Full Service - Early Clinical and Bioanalytical Solutions
Location
Missouri
Kansas
Lenexa
Kansas City, MO
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Facilities & Administratives Services
Clinic
Job Type
Permanent
Description
We are seeking a Clinical Dietary Aide to support meal service operations within our clinical research unit at ICON. In this role, you will help ensure that clinical trial participants receive meals a
Reference
JR148358
Expiry date
01/01/0001
Author
Lauren BerrettaAuthor
Lauren Berretta