PROGRAM DIRECTOR CCTO

Reposted One Month Ago
Be an Early Applicant
Bronx, NY, USA
In-Office
116K-145K Annually
Senior level
Healthtech
The Role
The Program Director oversees operations of the Early Phase Therapeutics oncology research program, including managing teams, ensuring compliance, and fostering industry partnerships.
Summary Generated by Built In

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 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 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 assures 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 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 Required

  • Master's degree in Life Science or Public Health
  • 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.
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The Company
HQ: New York, NY
9,797 Employees

What We Do

Montefiore is one of New York’s premier academic health systems, renowned for its leading medical school, groundbreaking research and technology, and highly specialized, coordinated care for diverse populations in the New York region, across the country and globally. Visit Montefiore.org to learn more.

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