Sr. Clinical Research Associate
Not Disclosed•Full-TimeOn-site
location_on1769, San Jacinto Street, Downtown, Houston, Harris County, Texas, 77002, United States
About ICON
ICON plc is a world-leading healthcare intelligence and clinical research organization. We are proud to foster an inclusive environment that drives innovation and excellence. Our mission is to shape the future of clinical development, and we welcome you to join us in this journey.
About the Role
As a Senior CRA at ICON, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. This role requires a strong foundation in clinical trial monitoring, offering the opportunity to work independently while guiding others.
You will lead on clinical trial monitoring tasks that demand technical depth, with a specific focus on quality and continuous improvement. In this position, you will build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations, ensuring successful execution across multiple sites.
Our Culture and Values
At ICON, inclusion and belonging are fundamental to our culture and values. We are dedicated to providing an inclusive and accessible environment for all candidates. Our success depends on the quality of our people, which is why we prioritize building a diverse culture that rewards high performance and nurtures talent.
ICON 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 you have a medical condition or disability and need a reasonable accommodation for any part of the application process, or to perform the essential functions of the position, please let us know or submit a request.
Application
Interested in the role but unsure if you meet all of the requirements? We encourage you to apply regardless—there is every chance you are exactly what we are looking for, whether for this role or others. If you are a current ICON employee, please apply through the internal portal.
Work location
Work model: On-site
1769, San Jacinto Street, Downtown, Houston, Harris County, Texas, 77002, United States
Houston, Texas
Similar Job Opportunities
Skills, education and keywords
Skills: Clinical Trial Monitoring, Good Clinical Practice, GCP, Ophthalmology, Clinical Trial Software.
Education: Bachelor's degree in a relevant scientific discipline or healthcare-related field required.
Frequently asked questions about Sr. Clinical Research Associate at Investigative Reporters and Editors
What does a Sr. Clinical Research Associate at Investigative Reporters and Editors do?expand_more
In this Sr. Clinical Research Associate at Investigative Reporters and Editors role, you will monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and gcp standards; conduct site visits to assess site performance, resolve issues, and provide support for successful trial execution; provide training and guidance to site staff and other cras to maintain high standards of clinical trial conduct; and build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
What are the requirements for this Sr. Clinical Research Associate role?expand_more
To qualify for the Sr. Clinical Research Associate at Investigative Reporters and Editors position, applicants should have: Bachelor's degree in a relevant scientific discipline or healthcare-related field; Extensive experience as a Clinical Research Associate; Ophthalmology experience required; and Willingness to travel approximately 60%.