ASSISTANT DIRECTOR FINANCE (JR227699)

ViziRecruiter,LLC.; New York (NY); On-site; USD 120,000 - 170,000; Full time

Job summary

Montefiore seeks an Assistant Director of Finance to lead the development, coordination and submission of Medicare Coverage Analyses and clinical trial budgets. You will prepare cost assessments for industry-sponsored trials and investigator-initiated studies, including foundation/grant-supported projects.

You will collaborate with program directors and staff to ensure billing compliance, reconciliation of accounts, and timely deployment of study start-up analyses.

Qualifications

• Master's degree in life science, public health, or business administration.
• Minimum 5 years related work experience with clinical trial budget development and negotiations.
• ACRP or SOCRA certification within 24 months of employment.
• Working knowledge of CMS guidelines and government codes related to human subject research.

Responsibilities

• Collaborate with Program Directors to oversee clinical research billing compliance.
• Coordinate development, coordination and submission of Medicare Coverage Analyses and trial budgets.
• Reconcile clinical research accounts and monitor start-up timelines with Regulatory Affairs.

Skills

Budget development

CMS guidelines

CTMS experience

Regulatory compliance

Communication skills

Negotiation

Education

Master's degree in life science, public health, or business administration

Tools

CTMS

EPIC

VELOS

COMPLION

Job description

Introduction

To heal, to teach, to discover and to advance the health of the communities we serve.

To learn more about the “Montefiore Difference” – who we are at Montefiore and all that we have to offer our associates, please click here.

Overview

Under the direction of the Sr.Directorof Cancer Clinical Research Administration, theAssistantDirectorofFinanceis 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.

Responsibilities

This position will collaborate with ProgramDirectors 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 theAssistantDirectorof 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