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PROGRAM DIRECTOR CCTO

new york, ny • Posted 6 days ago
Onsite Full Time Product Management

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 ProgramDirector is responsible for the daily operations, financial growth, and expansion of theEarly Phase Therapeuticsoncology clinical researchprogram. Expansion of theEarly Phase Therapeuticsclinical researchprogramcan include the physical expansion of theprogramacross multiple campuses, expansion of the capacity of clinical researchprogramthrough 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 (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 theEarly Phase Therapeutstrials, 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 researchprogramprinciple 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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