Research Coordinator I - Physician Practices Clinical Research -- Raleigh
Raleigh, North Carolina
Employer: WakeMed
Industry: Clinical Professional
Salary: Competitive
Job type: Full-Time
About WakeMed:
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
Position Information:
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.
Experience Requirements:
1 Year Clinical - Research Preferred
Education Required:
High School Diploma or Equivalent Required - And Bachelor's Degree Related Field Preferred
Licensure/Certification Requirements:
Certified Clinical Research Coordinator Or Certified Clinical Research Professional Preferred
Hours of Work:
Monday-Friday, day
Weekend Requirements:
No Weekends
Call Requirements:
N/A
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
Position Information:
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.
Experience Requirements:
1 Year Clinical - Research Preferred
Education Required:
High School Diploma or Equivalent Required - And Bachelor's Degree Related Field Preferred
Licensure/Certification Requirements:
Certified Clinical Research Coordinator Or Certified Clinical Research Professional Preferred
Hours of Work:
Monday-Friday, day
Weekend Requirements:
No Weekends
Call Requirements:
N/A
Created: 2024-06-17
Reference: 56461
Country: United States
State: North Carolina
City: Raleigh
ZIP: 27617
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