MGR CLINICAL TRIALS OFFICE

This position will be on site/remote

This will be for our BMT team.

Position Highlights:

• Responsible for the direct supervision of clinical research staff
• Leads the daily clinical research operations for one or more key areas
• Responsible for monitoring workloads and determining appropriate staffing levels for the clinical research staff (nurses, coordinators, and data specialists)
• Takes the lead and/or participates in development and execution of training/mentoring programs, quality improvement processes and other projects, including the development of SOP's
• Works in collaboration with the Clinical Trials Business Office and Research Finance to coordinate budget development and research patient and sponsor billing
• Responsible for budgeting and financial management of one or more cost centers

Responsibilities:

• Staff supervision and mentoring, monitor staff conduct, perform staff interviews, recommend hire/terminations, and perform annual staff evaluations
• Allocates staff based on patient acuity, staffing standards and expertise of personnel
• Fiscal oversight-develop annual budget for the Clinical Trials Office cost center, review individual protocol budgets to assure adequate data management reimbursement; responsible for revenue creation, cost management and purchasing
• Actively participate in operational review of new protocols and amendments for feasibility of conduct
• Assist with development, revision and continuous evaluation of clinical research department standards and policies; participate in and/or lead process improvement working groups and staff mentoring education activities

Credentials and Qualifications:

• Bachelor's degree (Master's preferred)
• Five (5) years of experience in executing multidisciplinary clinical research protocols (preferably in oncology)
• Two (2) years of staff supervisory/management experience
• Clinical Research Certification (e.g. SOCRA, ACRP) preferred