WakeMed
WakeMed
Posted 1 day ago
Full Time
Raleigh, North Carolina
In Person
Smart Summary
Responsibilities
The Research Coordinator I assists investigators with the planning and implementation of clinical trials, including subject recruitment and consent. They are also responsible for managing research documentation, billing reviews, IRB submissions, and monitoring clinical trial activities.
Qualifications
You have a High School Diploma or equivalent and 1 year of clinical research experience. You will assist investigators and the research team with planning and implementing clinical trials, including subject recruitment, consent, and data collection.
Must Have Skills for ATS
CRF completion
IRB submissions
adverse event reporting
protocol deviation reporting
Job Description
Serving the community since 1961, WakeMed Health & Hospitals is the leading provider of health services in Wake County. With a mission to improve the health and well-being of our community, we are committed to providing outstanding and compassionate care. For more information, visit www.wakemed.org.
EOE
WakeMed
With Runway
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