At Moffitt Cancer Center, we strive to be the leader in understanding the complexity of cancer and applying these insights to contribute to the prevention and cure of cancer. Our diverse team of over 9,000 are dedicated to serving our patients and creating a workspace where every individual is recognized and appreciated. For this reason, Moffitt has been recognized on the 2023 Forbes list of America’s Best Large Employers and America’s Best Employers for Women, Computerworld magazine’s list of 100 Best Places to Work in Information Technology, DiversityInc Top Hospitals & Health Systems and continually named one of the Tampa Bay Time’s Top Workplace. Additionally, Moffitt is proud to have earned the prestigious Magnet® designation in recognition of its nursing excellence. Moffitt is a National Cancer Institute-designated Comprehensive Cancer Center based in Florida, and the leading cancer hospital in both Florida and the Southeast. We are a top 10 nationally ranked cancer center by Newsweek and have been nationally ranked by U.S. News & World Report since 1999.
Working at Moffitt is both a career and a mission: to contribute to the prevention and cure of cancer. Join our committed team and help shape the future we envision.

Summary

We are seeking an exceptional leader to join our team with strong background in leading teams through the processes of Budget Development and Clinical Trials negotiations. The ideal candidate will have a proven ability to achieve significant reductions in activation times. Experience in early therapeutics is highly desirable.

Key Responsibilities:

- Lead and mentor teams in the development and negotiation of clinical trial budgets.

- Drive initiatives that enhance activation times and overall project efficiency.

- Collaborate with cross-functional teams to ensure successful trial execution.

Qualifications:

- Strong leadership skills with a history of successful team development

- Demonstrated experience in clinical trial budget development and negotiation.

- Demonstrated success in improving activation timelines.

The Director, Clinical Trial Business Office is responsible for providing leadership and has general
oversight of the Clinical Trial Business Office functions including Contracts, Budgets, Coverage analysis,
Clinical Trial Management System calendars and post activation amendments.
The Director, Clinical Trial Business office is the signatory authority to clinical trial agreements, Letter of
Indemnification, sub-sites and Master agreements. The Director is responsible for ensuring Clinical Trial
Business Office efforts are in compliance with the Center's guidelines, state and federal regulations by
monitoring and evaluating the quality and appropriateness of the department activities.
A successful Director, Clinical Trial Business Office promotes and supports the clinical trial infrastructure
to advance clinical trial activation, study management and provides support to principal investigators,
clinical research and revenue cycle personnel. The Director works proactively and collaborates with
various departments across the organization to design efficient and compliant operational workflows to
achieve activation and revenue targets.

Minimum Experience Required
• Minimum of eight (8) years of healthcare or related industry experience in clinical research business
functions (contracting, budgeting, negotiating, clinical trial management systems and/or Coverage
Analysis development) of academic medical centers
• Minimum of three (3) years supervisory experience
Minimum Skills/Specialized Training Required
• Leadership and mentoring skills necessary to provide support to department and promote employee
development
• Outstanding verbal and written communication skills to support interaction and participation in meetings
with patients, physicians, payer representatives, affiliates, oncology partners, and representatives of
another internal department.
• Proven analytical ability and organizational skills necessary to organize/assess information and evaluate
recommendations based on data analysis

• Strong focus on compliance and building a complaint department including establishing working
relationships with
Internal Audit and Corporate Compliance
• Working knowledge of federal grant management policies and regulation governing sponsored
agreements, clinical trial policy and federal billing guidelines
• Proficient in problem-solving, project management, multi-tasking and time management.
• Proficient business software skills including Microsoft Office
Preferred Experience
Experience in oncology related research operations of large academic institutions and NCI designated
cancer center
Preferred in-depth knowledge of research business operations, use of technology to improve efficiency of
operations and an advocate of change leading to improved processes
Preferred Skills/Specialized Training
Advarra Research System's Oncore Clinical Trials Management System knowledge
Cerner Millennium knowledge
Cerner Soarian Financials knowledge

Minimum Education

Bachelor's Degree Business, Public Health,
Healthcare related or similar field
Preferred Education

Master's Degree MBA, MHA, scientific related
Master's degree