Clinical Coordinator
University of Vermont, Burlington, VT, United States
Clinical Coordinator
Posting Summary
Coordinate and manage clinical research protocols for the Vaccine Testing Center (VTC) within the Department of Microbiology and Molecular Genetics. Serve as a key liaison among investigators, sponsors, regulatory bodies, and clinical partners. Support study start-up, implementation, and closeout activities with a primary focus on the day-to-day, clinic-based operations of assigned studies. This includes coordinating participant visits, supporting recruitment and enrollment, and collaborating with the clinical team to ensure smooth study execution. Prepare regulatory submissions and study documentation. Support study operations, data quality, and participant safety by coordinating study activities, maintaining study records, and adhering to protocol requirements. Contribute to improving processes and assist with training of new staff as needed.
Minimum Qualifications (or equivalent combination of education and experience)
Bachelor's degree with a scientific background and three to five years' related experience required. Effective interpersonal communication skills and time management skills essential. Training and/or certification as a clinical research coordinator, such as Good Clinical Practices (GCP), or the ability to obtain.
Anticipated Pay Range
$57,000-$62,000
Special Conditions
A probationary period may be required, contingent on continued funding, occasional evening and/or weekends required (if non-exempt position, may result in overtime). This position is ineligible for telework due to the essential functions, background check required for this position.
FLSA
Exempt
Union Position
Yes, UVMSU
Job Location
Burlington, Vermont, United States
Standard Hours at 1.0 FTE
37.5
Term (months per year)
12
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Posting Summary
Coordinate and manage clinical research protocols for the Vaccine Testing Center (VTC) within the Department of Microbiology and Molecular Genetics. Serve as a key liaison among investigators, sponsors, regulatory bodies, and clinical partners. Support study start-up, implementation, and closeout activities with a primary focus on the day-to-day, clinic-based operations of assigned studies. This includes coordinating participant visits, supporting recruitment and enrollment, and collaborating with the clinical team to ensure smooth study execution. Prepare regulatory submissions and study documentation. Support study operations, data quality, and participant safety by coordinating study activities, maintaining study records, and adhering to protocol requirements. Contribute to improving processes and assist with training of new staff as needed.
Minimum Qualifications (or equivalent combination of education and experience)
Bachelor's degree with a scientific background and three to five years' related experience required. Effective interpersonal communication skills and time management skills essential. Training and/or certification as a clinical research coordinator, such as Good Clinical Practices (GCP), or the ability to obtain.
Anticipated Pay Range
$57,000-$62,000
Special Conditions
A probationary period may be required, contingent on continued funding, occasional evening and/or weekends required (if non-exempt position, may result in overtime). This position is ineligible for telework due to the essential functions, background check required for this position.
FLSA
Exempt
Union Position
Yes, UVMSU
Job Location
Burlington, Vermont, United States
Standard Hours at 1.0 FTE
37.5
Term (months per year)
12
#J-18808-Ljbffr