UVMCC CTO Quality Assurance Officer
Full Time
Burlington, VT 05401
Posted
Job description
Building Name: UVMMC - Medical Center - Main Campus
Location Address: 111 Colchester Avenue, Burlington Vermont
Regular
Department: Oncology Clinical Trials
Full Time
Standard Hours: 40
Shift: Day/Eve-8Hr
Primary Shift: 8:00 AM - 4:30 PM
Weekend Needs: None
Salary Range: Min $33.72 Mid $42.15 Max $50.57
Recruiter: Naomi Kpesse
EDUCATION:
We are the heart and science of medicine. We are UVM Medical Center.
This position is responsible for developing, establishing, monitoring, and ensuring on-going compliance to quality standards for the conduct of all cancer clinical research studies within The University of Vermont Cancer Center Clinical Trials Office (UVMCC CTO) and network affiliates. They are responsible for developing and implementing a quality management program related to the execution of clinical trials and monitoring adherence to policies and applicable regulations. This position will assist with the development and implementation of organizational corrective and preventive action plans and Standard Operating Procedures based on internal and external monitoring and audit findings. They are also responsible for identifying areas needing additional training and education and assisting with the development of those resources. This position will evaluate the effectiveness of the quality assurance program and provide regular updates to the UVMCC CTO Director, Medical Director, and cancer center leadership. This position will develop and implement a cancer center clinical trials program orientation for new physicians, investigators, research coordinators, and lead cancer clinical trials education initiatives. The position will conduct quality assurance monitoring to ensure compliance to clinical trials quality standards at UVMCC CTO and network affiliates. They are also responsible for oversight of UVMCC Data and Safety Monitoring Committee (DSMC) operations.
EDUCATION:
BA/BS required. Must be eligible for certification by professional organization in the area of clinical research. Current certification in SoCRA or ACRP preferred.
EXPERIENCE:
Minimum 5 years’ experience with cancer clinical trials required. Experience with quality assurance, clinical trial auditing/monitoring, and good clinical practice. Experience in protocol development and working with investigator-initiated studies highly preferred. Experience working with PRMCs and DSMCs highly preferred. Experience working at an NCI designated cancer center highly preferred.
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