ASSISTANT DIRECTOR FINANCE
At a glance
Director-level Finance Leadership role at Montefiore. 111 East 210th Street · full-time · $120,000–$150,000 base.
financeroles summary, based on the employer's posting.
What you'll do
- Build and submit Medicare coverage reviews and trial budgets, including detailed cost estimates for sponsored and grant-supported studies
- Work with program directors to keep oncology research billing aligned with applicable rules
- Reconcile clinical research accounts and coordinate study-startup tracking with regulatory affairs
- Coordinate regularly with faculty, research nurses, study coordinators, sponsors and departmental staff
What you bring
- A master's degree in life science, public health or business administration
- At least five years developing and negotiating budgets for clinical trials
- ACRP or SOCRA certification within two years of starting
- Working knowledge of human-subject research rules and CMS guidance
Who this fits
This role suits someone with clinical trial finance experience who can manage budgets, compliance and account reconciliation. It is a weekday daytime schedule in the Bronx, New York, and the role is grant-funded.
From the employer
City/State:
Bronx, New YorkGrant Funded:
YesDepartment:
Cancer Clinical Trials OfficeWork Shift:
DayWork Days:
MON-FRIScheduled Hours:
9 AM-5:30 PMScheduled Daily Hours:
7.5 HOURSPay Range:
$120,000.00-$150,000.00Under the direction of the Sr. Director of Cancer Clinical Research Administration, the Assistant Director of Finance is responsible for the development, coordination and submission of Medicare Coverage Analyses, clinical trial budgets; preparing detailed cost assessments for industry sponsored clinical trials and investigator-initialed studies, including studies support by foundations and grants.
This position will collaborate with Program Directors to oversee clinical research billing compliance for oncology studies ensuring compliance with local, state and federal regulations. This position will be responsible for the reconciliation of clinical research accounts.
This position will collaborate with the Assistant Director of Regulatory Affairs to monitor and track Time to Activation of study start-up. This position will interact on a regular basis with faculty, research nurses, study coordinators, departmental offices, outside sponsors, and other relevant staff.
Requirements
Master's degree required in life science, public health, or business administration
Minimum of 5 years related work experience with clinical trial budget development and negotiations
ACRP or SOCRA required within 24 months of employment
Working knowledge of local, state, federal and international government codes/regulations related to the conduct of human subject research and CMS guidelines
Extensive experience with CTMS and other clinical trial electronic systems (CTMS, EPIC, VELOS, COMPLION) are highly desirable
Exceptional communication, analytical, presentation and time management skills
Montefiore Medical Center is an equal employment opportunity employer. Montefiore Medical Center will recruit, hire, train, transfer, promote, layoff and discharge associates in all job classifications without regard to their race, color, religion, creed, national origin, alienage or citizenship status, age, gender, actual or presumed disability, history of disability, sexual orientation, gender identity, gender expression, genetic predisposition or carrier status, pregnancy, military status, marital status, or partnership status, or any other characteristic protected by law.