Sr. Clinical Research Associate
Not Disclosed•Full-TimeOn-site
location_on577, Mallard Avenue, Durham, Durham County, North Carolina, 27701, 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 is designed for a professional with a strong foundation in clinical trial monitoring who can work independently while guiding others.
You will lead on clinical trial monitoring tasks requiring 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. Your work will involve collaborating with cross-functional teams to ensure timely and accurate data collection and reporting, while also providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
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 have made it a priority to build 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, 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 or submit a request.
Application
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there's every chance you're exactly what we're looking for here at ICON, whether it is for this or other roles.
If you are a current ICON employee, please apply via the internal careers site.
Work location
Work model: On-site
577, Mallard Avenue, Durham, Durham County, North Carolina, 27701, United States
Durham, North Carolina
Key Responsibilities
- check_circleMonitor clinical trial sites to ensure adherence to protocols and GCP standards
- check_circleConduct site visits to assess performance and resolve issues
- check_circleProvide training and guidance to site staff and other CRAs
- check_circleBuild and maintain effective relationships with site personnel and stakeholders
- check_circleCollaborate with cross-functional teams for accurate data collection and reporting
Requirements
- verifiedBachelor's degree in a relevant scientific discipline or healthcare-related field
- verifiedExtensive experience as a Clinical Research Associate
- verifiedOphthalmology experience required
- verifiedWillingness to travel approximately 60%
Benefits & Perks
check_circleVarious annual leave entitlementscheck_circleA range of health insurance offerings for you and your familycheck_circleCompetitive retirement planning offerings to maximize savingscheck_circleGlobal Employee Assistance Programme via TELUS Health with 24-hour accessLife assurance coverage
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.
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
A Sr. Clinical Research Associate at Investigative Reporters and Editors is responsible for the following: Monitor clinical trial sites to ensure adherence to protocols and GCP standards; Conduct site visits to assess performance and resolve issues; Provide training and guidance to site staff and other CRAs; and Build and maintain effective relationships with site personnel and stakeholders.
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%.
Where is the Sr. Clinical Research Associate role at Investigative Reporters and Editors located?expand_more
Sr. Clinical Research Associate at Investigative Reporters and Editors is based in 577, Mallard Avenue, Durham, Durham County, North Carolina, 27701, United States. This is a on-site role.
Is this Sr. Clinical Research Associate job remote, hybrid, or on-site?expand_more
Investigative Reporters and Editors has listed this Sr. Clinical Research Associate role as on-site.
How much experience is required for this Sr. Clinical Research Associate role?expand_more
Candidates for Sr. Clinical Research Associate at Investigative Reporters and Editors should have senior.
What skills do you need for the Sr. Clinical Research Associate role at Investigative Reporters and Editors?expand_more
Key skills for Sr. Clinical Research Associate at Investigative Reporters and Editors include Clinical Trial Monitoring; Good Clinical Practice; GCP; Ophthalmology; and Clinical Trial Software.
What education is required for Sr. Clinical Research Associate at Investigative Reporters and Editors?expand_more
Educational requirements for this role: Bachelor's degree in a relevant scientific discipline or healthcare-related field.
What category does the Sr. Clinical Research Associate role belong to?expand_more
Sr. Clinical Research Associate at Investigative Reporters and Editors is part of the scientific & qa job category on Recrutus.