Mgr Clinical Trials Office

Summary

This position will be on site/remote. It will be for our BMT team.

• Direct supervision of clinical research staff.
• Lead daily clinical research operations for one or more key areas.
• Monitor workloads and determine appropriate staffing levels for staff (nurses, coordinators, data specialists).
• Take the lead and/or participate in development and execution of training/mentoring programs, quality improvement processes and other projects, including development of SOPs.
• Collaborate 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.
• Staff supervision and mentoring, monitor staff conduct, perform staff interviews, recommend hire/terminations, and perform annual staff evaluations.
• Allocate 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.

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

Mid-Senior level

Full-time

Research, Analyst, and Information Technology

Hospitals and Health Care