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PROGRAM DIRECTOR CCTO

111 East 210th StreetOn-siteFull-time

AI Summary

Oversees the daily operations, financial growth, and expansion of the Early Phase Therapeutics oncology clinical research program across multiple campuses, supervising data managers, research associates, and technicians.

About this role

City/State:

Bronx, New York

Grant Funded:

Yes

Department:

Cancer Clinical Trials Office

Work Shift:

Day

Work Days:

MON-FRI

Scheduled Hours:

9 AM-5:30 PM

Scheduled Daily Hours:

7.5 HOURS

Pay Range:

$116,000.00-$145,000.00

The Program Director is responsible for the daily operations, financial growth, and expansion of theEarly Phase Therapeuticsoncology clinical research program. Expansion of theEarly Phase Therapeuticsclinical research program can include the physical expansion of the program across multiple campuses, expansion of the capacity of clinical research program through the development of a research specific unit, and 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 (Program Leaders, 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 theEarly Phase Therapeuticstrials, 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 < 90 days.

Review Medicare coverage analysis for appropriate procedure level designations

Serve as theEarly Phase Therapeuticsclinical research program principle liaison with pharmaceutical and biotechology companies

Prepare for NIH, BRANY and Sponsor audits and FDA inspections

Serve on departmental and institutional committees as necessary

Other duties as assigned

Requirements/Qualifications

Master's degree in Life Science or Public Health required

5 year's 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

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.

Skills

ACRP CertificationBilling ComplianceBRANY Audit PreparationCITI TrainingClinical Trials ManagementData ManagementEarly Phase Drug DevelopmentFDA Inspection PreparationFederal RegulationsIATALocal RegulationsMedicare Coverage AnalysisNIH Audit PreparationOncology Clinical ResearchProtocol Start-up ManagementRegulatory ComplianceResearch CoordinationSOCRA Certification

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