Introduction
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Overview Under the direction of the Sr.Directorof Cancer Clinical Research Administration, the AssistantDirectorofFinance 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.
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 also be responsible for the reconciliation of clinical research accounts.
This position will collaborate with the AssistantDirectorof Regulatory Affairs to monitor and track Time to Activation of study start‑up. The role 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
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Overview Under the direction of the Sr.Directorof Cancer Clinical Research Administration, the AssistantDirectorofFinance 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.
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 also be responsible for the reconciliation of clinical research accounts.
This position will collaborate with the AssistantDirectorof Regulatory Affairs to monitor and track Time to Activation of study start‑up. The role 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
#J-18808-Ljbffr