Accessability Links
Cookies on our website
By continuing to use this website we will assume you are happy to receive cookies as outlined in our cookie policy
Accept Policy

Clinical Research Coordinator

US-Texas-San Antonio, IDS
Reference: 060540_2
This vacancy has now expired.

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.

Similar jobs
Associate Epidemiologist/Junior Biostatistician



View Job Shortlist


San Francisco,Arizona,Nevada


View Job Shortlist


Back to Top