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Program Director Ccto

Job in Bronx, Bonner County, Idaho, USA
Listing for: Dormont Manufacturing Co
Full Time position
Listed on 2026-07-11
Job specializations:
  • Healthcare
  • Management
Salary/Wage Range or Industry Benchmark: 116000 - 145000 USD Yearly USD 116000.00 145000.00 YEAR
Job Description & How to Apply Below
Position: PROGRAM DIRECTOR CCTO
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
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.

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