Not specified; competitive within country; range o...
Onsite
Bachelor's degree required
1+ years crc experience
Protocol compliance and safety monitoring
The role involves ensuring participant safety while actively recruiting suitable candidates for clinical trials at the Raleigh site
Job Summary
The role involves ensuring participant safety while actively recruiting suitable candidates for clinical trials at the Raleigh site.
The coordinator is responsible for performing technical study procedures such as phlebotomy, ECGs, and pulmonary function testing as ordered by the investigator.
ICON offers a competitive salary, diverse benefits including health insurance and retirement planning, and a culture focused on inclusion and belonging.
Matching Summary
The role involves ensuring participant safety while actively recruiting suitable candidates for clinical trials at the Raleigh site.
Salary
Not specified; Competitive within country; Range of additional benefits offered
Skills & Requirements
Must-have
Bachelor's Degree required
1+ years CRC experience
Protocol compliance and safety monitoring
Patient recruitment and screening
Source document creation and maintenance
Adverse event reporting to IRB
Electronic Data Capture (EDC) entry
Nice-to-have
Strong attention to detail
Interest in clinical research career
Mentoring and staff development skills
Ability to work autonomously
Building strong investigator relationships
Key Requirements
Bachelor's Degree
1+ years of Clinical Research Coordinator experience