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.
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