{"schemaVersion":"jobsearcher.job.v1","id":"17536bc95841cca1defc2886","url":"https://jobsearcher.com/jobs/17536bc95841cca1defc2886","canonicalUrl":"https://jobsearcher.com/jobs/17536bc95841cca1defc2886","title":"PROGRAM DIRECTOR CCTO","description":"City/State:\n\nBronx, New York\n\nGrant Funded:\n\nYes\n\nDepartment:\n\nCancer Clinical Trials Office\n\nWork Shift:\n\nDay\n\nWork Days:\n\nMON-FRI\n\nScheduled Hours:\n\n9 AM-5:30 PM\n\nScheduled Daily Hours:\n\n7.5 HOURS\n\nPay Range:\n\n$116,000.00-$145,000.00\n\nThe 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.\n\nThis position will oversee daily operations across multiple campuses including the direct supervision of data managers, research associates, and research technicians.\n\nResponsibilities\n\nResponsible for training and on-boarding of new study coordinators\n\nWork 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\n\nResponsible 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\n\nManage clinical trials portfolio and assures timely start-up of protocols to maintain NCI expectations of < 90 days.\n\nReview Medicare coverage analysis for appropriate procedure level designations\n\nServe as the Early Phase Therapeutics clinical research program principle liaison with pharmaceutical and biotechology companies\n\nPrepare for NIH, BRANY and Sponsor audits and FDA inspections\n\nServe on departmental and institutional committees as necessary\n\nOther duties as assigned\n\nRequirements/Qualifications\n\nMaster's degree in Life Science or Public Health required\n\n5 year's related work experience\n\nACRP or SOCRA certification within 24 months of employment\n\nMD, DDS (or foreign equivalent) degree preferred\n\nPrior Clinical research experience in early phase drug development\nKnowledge of Federal and local regulations.\nCITI\n\nIATA\n\nMontefiore 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.","company":"Montefiore Einstein","rawCompany":"montefiore einstein","city":"Bronx","state":"NY","isRemote":false,"isActive":false,"createdAt":"2026-08-29T09:44:45.320Z","occupations":[{"code":"11-9121.01","title":"Clinical Research Coordinators","slug":"clinical-research-coordinators"},{"code":"11-9111.00","title":"Medical and Health Services Managers","slug":"medical-and-health-services-managers"},{"code":"11-9151.00","title":"Social and Community Service Managers","slug":"social-and-community-service-managers"}],"industries":[{"code":"541715","title":"Research and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)","slug":"research-and-development-in-the-physical-engineering-and-life-sciences-except-nanotechnology-and-biotechnology"},{"code":"923120","title":"Administration of Public Health Programs","slug":"administration-of-public-health-programs"},{"code":"541714","title":"Research and Development in Biotechnology (except Nanobiotechnology)","slug":"research-and-development-in-biotechnology-except-nanobiotechnology"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"PROGRAM DIRECTOR CCTO","description":"City/State:\n\nBronx, New York\n\nGrant Funded:\n\nYes\n\nDepartment:\n\nCancer Clinical Trials Office\n\nWork Shift:\n\nDay\n\nWork Days:\n\nMON-FRI\n\nScheduled Hours:\n\n9 AM-5:30 PM\n\nScheduled Daily Hours:\n\n7.5 HOURS\n\nPay Range:\n\n$116,000.00-$145,000.00\n\nThe 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.\n\nThis position will oversee daily operations across multiple campuses including the direct supervision of data managers, research associates, and research technicians.\n\nResponsibilities\n\nResponsible for training and on-boarding of new study coordinators\n\nWork 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\n\nResponsible 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\n\nManage clinical trials portfolio and assures timely start-up of protocols to maintain NCI expectations of < 90 days.\n\nReview Medicare coverage analysis for appropriate procedure level designations\n\nServe as the Early Phase Therapeutics clinical research program principle liaison with pharmaceutical and biotechology companies\n\nPrepare for NIH, BRANY and Sponsor audits and FDA inspections\n\nServe on departmental and institutional committees as necessary\n\nOther duties as assigned\n\nRequirements/Qualifications\n\nMaster's degree in Life Science or Public Health required\n\n5 year's related work experience\n\nACRP or SOCRA certification within 24 months of employment\n\nMD, DDS (or foreign equivalent) degree preferred\n\nPrior Clinical research experience in early phase drug development\nKnowledge of Federal and local regulations.\nCITI\n\nIATA\n\nMontefiore 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.","datePosted":"2026-08-29T09:44:45.320Z","dateModified":"2026-08-29T09:44:45.320Z","hiringOrganization":{"@type":"Organization","name":"Montefiore Einstein","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Bronx","addressRegion":"NY","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"17536bc95841cca1defc2886"},"url":"https://jobsearcher.com/jobs/17536bc95841cca1defc2886"}}