Joining our team comes with several benefits, including:

• Competitive hourly rate

   

• Free parking
• Tuition reimbursement

A Brief Overview
 

Provides departmental management interface and quality assurance expertise to ensure departmental compliance with regulatory and accreditation agencies. Supports quality assurance activities for both the Cellular Therapy and Heme Malignancy Programs within the Seidman Cancer Center. Implements and facilitates quality goals based on the clincial and laboratory program Quality Plans.

What You Will Do
 

• Quality review of medical and lab records associated with cellular therapy procedures and treatments.
• Assists with writing, revising, and maintenance of standard operating procedures and associated forms and worksheets; facilitates reviews and approvals; ensures protocol compliance
• NMDP Executes internal audits, coordinate and prepares for external audits including FACT, FDA, Joint Commission, ODH and commercial partners who provide therapeutic products to the program.
• Collaborates with interdepartmental staff on quality improvement projects. Reviews and facilitates incident/accident/errors. Corrective action/follow up
• Ensures programmatic compliance including but not limited to FDA, FACT (Foundation for the Accreditation of Cellular Therapy), NMDP, CIBMTR, ODH, JC.

Additional Responsibilities
 

• Performs other duties as assigned.
• Complies with all policies and standards.
• For specific duties and responsibilities, refer to documentation provided by the department during orientation.
• Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.