Montefiore Medical Center
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 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 onboarding 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 assure timely start-up of protocols to maintain NCI expectations of
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 required 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 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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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 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 onboarding 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 assure timely start-up of protocols to maintain NCI expectations of
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 required 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 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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