Clinical Research Coord II Hem/Onc

University of Vermont Medical Center; Burlington (VT); On-site; USD 55,000 - 90,000; Full time

Job summary

The University of Vermont Medical Center seeks a Clinical Research Coordinator II to coordinate and implement clinical and non-clinical tasks for multiple research protocols, ensuring compliance and quality.

Associate degree required; bachelor preferred. At least two years coordinating research protocols independently with relevant medical experience. The role may operate with direction from the Principal Investigator.

Qualifications

• Associates Degree required or equivalent technical certification (e.g., EMT, EKG Technician, Medical Assistant).
• Bachelor degree preferred.
• At least two years of experience coordinating research protocols independently with relevant medical experience.

Responsibilities

• Coordinate and implement clinical and non-clinical tasks for multiple protocols.
• May function independently with direction from the Principal Investigator and research leadership.

Education

Associates Degree required or equivalent technical certification (e.g., EMT, EKG Technician, Medical Assistant).

Bachelor degree preferred

Job description

JOB DESCRIPTION:

The Clinical Research Coordinator II coordinates and implements vital clinical and non-clinical tasks related to the successful completion of multiple research protocols consistent with knowledge and experience. A successful Clinical Research Coordinator II requires specialized knowledge and skills that are acquired through experience and/or education. This position should be extramurally funded therefore continued employment is largely dependent on the availability of funds in addition to satisfactory performance. The position may function independently with direction from the Principal Investigator and other research leadership staff.

EDUCATION:

Associates Degree required or equivalent technical certification (e.g., EMT, EKG Technician, Medical Assistant). Bachelor degree preferred.

EXPERIENCE:

At least two years of experience coordinating research protocols independently and appropriate relevant medical experience.