Program Director Ccto

Position: PROGRAM DIRECTOR CCTO
Location: New York

PROGRAM DIRECTOR CCTO page is loaded## PROGRAM DIRECTOR CCTOlocations: 111 East 210th Streettime type:
Full time posted on:
Posted Todayjob requisition
** 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 malignant hematology oncology clinical research program. Expansion of the Malignant Hematology 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 hematologic malignancy 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 hematologic malignancy 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 required5 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. CITIIATAMontefiore 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.###

EMPLOYEE BENEFITS An assortment of insurance products and discount programs through Voluntary Benefits.

Check out our comprehensive available to you when you join our outstanding team! #J-18808-Ljbffr