Clinical Research Assistant, Aortic Center
1 month ago
How You'll Help Transform Healthcare:
Under general supervision of the Principal Investigator, assists with administrative activities associated with the conduct of research studies including industry-sponsored, grant-funded, or internally-funded studies.
This position will be assigned to serve in a support minimal risk or non-interventional studies unless assigned to serve in a support function for greater than minimal risk studies that also include a Clinical Research Coordinator.
This person will be assigned to the Aortic Center focusing on vascular surgery. The primary responsibility of this CRA will be to work on investigator-initiated research developing and utilizing the FEVAR database. This is an ideal position for a self-motivated individual interested in pursuing a career in medicine.- Under supervision of Principal Investigator, assist in overseeing compliance to research protocols.
- Communicates with study team, research sponsor or CRO, local or central IRB, Office of Sponsored Projects, and other ancillary departments to ensure smooth implementation of research protocol and ongoing maintenance.
- Assist in monitoring enrollment goals.
- Collects data from patient charts, medical records, interviews, questionnaires, diagnostic tests and other sources.
- Ensure compliance with protocol guidelines and requirements of regulatory agencies.
- Under supervision of Principal Investigator, coordinates all site related monitoring or auditing visits from sponsor and/or federal agency during the course of the study and at closure.
- Prepares, submits and maintains IRB, OSP, FDA and/or any other funding or regulatory documents and research correspondence.
- Develops and maintains patient databases and study maintenance logs including but not limited to training logs, delegation of responsibility logs, screening logs, and enrollment logs.
What We Require:
Education:
Bachelor's Degree required. Bachelor's Degree in Science or a related field required. Three (3) years experience in clinical research may be substituted for education.
Experience: 1 year in healthcare or research preferred.
Licensure, certification, and/or registration:
IATA required with hire.
Other Minimum Qualifications:
Excellent computer skills; strong knowledge of word processing, spreadsheets, databases, and internet environment. Knowledge of medical and/or pharmaceutical terminology strongly desired. Strong organization and communication skills required. Able to work with multiple interruptions and to perform multiple tasks at any given time.
About Carilion
This is Carilion Clinic ...
An organization where innovation happens, collaboration is expected and ideas are valued. A not-for-profit, mission-driven health system built on progress and partnerships. A courageous team that is always learning, never discouraged and forever curious.
Headquartered in Roanoke, Va., you will find a robust system of award winning hospitals, Level 1 and 3 trauma centers, Level 3 NICU, Institute of Orthopedics and Neurosciences, multi-specialty physician practices, and The Virginia Tech Carilion School of Medicine and Research Institute.
Requisition Number:
#
Employment Status:
Full time
Location:
Carilion Clinic - Crystal Spring
Shift:
Day
Shift Details:
Monday through Friday, dayshift; could be occasions to work other days/hours
For more information, contact the HR Service Center at
Equal Opportunity Employer
Minorities/Females/Protected Veterans/Individuals with Disabilities/Sexual Orientation/Gender Identity
Carilion Clinic is a drug-free workplace.
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