WakeMed - Raleigh, NC
posted 3 days ago
Full-time - Entry Level
Raleigh, NC
Hospitals
About the position
The Research Coordinator I will assist the Investigators and research team with the planning and implementation of clinical trials. This includes, but is not limited to, subject recruitment, consent, research procedures (as appropriate), CRF completion, communication and meeting with sponsor representatives, scheduling and assisting with clinical trial monitoring activities, completing research billing reviews, completing IRB submissions and reporting of adverse events and protocol deviations.
Responsibilities
- Assist Investigators and research team with planning and implementation of clinical trials
- Subject recruitment and consent
- Conduct research procedures as appropriate
- Complete CRF (Case Report Form)
- Communicate and meet with sponsor representatives
- Schedule and assist with clinical trial monitoring activities
- Complete research billing reviews
- Complete IRB (Institutional Review Board) submissions
- Report adverse events and protocol deviations
Requirements
- Certified Clinical Research Coordinator or Certified Clinical Research Professional
- High School Diploma or Equivalent Required
- 1 Year Clinical - Research Preferred
Nice-to-haves
- Bachelor's Degree in a Related Field Preferred
