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PROGRAM DIRECTOR CCTO (JR227774)

ViziRecruiter,LLC.
CompanyViziRecruiter,LLC.
CategoryUncategorised
LocationNew York
RemoteOn-site (inferred)
EmploymentNot stated
LevelNot stated
SalaryNot stated by the employer
Posted9 Aug 2026
Last verified12 Aug 2026
SourceThe employer's own careers page (company_site)
Applications are handled by the employer, not by us.Apply on the employer's site →
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 The Program Director is responsible for the daily operations, financial growth, and expansion of the Early Phase Therapeutics oncology clinical research program. Expansion of the Early Phase Therapeutics clinical research program can include the physical expansion of the program across multiple campuses, the expansion of the capacity of the clinical research program through the development of a research specific unit, and the cultivation of relationships with key industry partners. This position will oversee daily operations across multiple campuses including the direct supervision of data managers, research associates and research technicians. Responsibilities • Responsible for training and on-boarding of new study coordinators. • Work closely with research team (ProgramLeaders, co-investigators, research coordinators, research nurses, other data managers, and protocol office staff) in the management of each patient that is accrued to a study. • Responsible for the billing compliance of the Early Phase Therapeutics trials, ensuring the proper ordering and association of consult and ancillary services (laboratory tests, imaging, etc.) as well as reviewing charges and designations once the visit is closed • Manage clinical trials portfolio and assures timely start-up of protocols to maintain NCI expectations of Requirements • Master's degree in Life Science or Public Health required. • 5 years' related work experience. • ACRP or SOCRA certification within 24 months of employment. • MD, DDS (or foreign equivalent) degree preferred. • Prior Clinical research experience in early phase drug development. • Knowledge of Federal and local regulations. • CITI. • IATA. #J-18808-Ljbffr