Program Director Ccto
Listed on 2026-07-11
-
Healthcare
-
Management
Location: Bronx
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:
$-$
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, expansion of the capacity of the 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 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 assure timely start‑up of protocols to maintain NCI expectations of < 90 days
- Review Medicare coverage analysis for appropriate procedure level designations
- Serve as the Early Phase Therapeutics clinical research program principal 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
- 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.
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