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Research CoordinatorCompany Albert Einstein College of Medicine
Location Bronx, NY
Update 10 Day ago
Einstein’s major strength, in addition to training physicians and scientists, is its science. During fiscal year 2015, the faculty’s consistently high level of scientific achievement resulted in the awarding of more than $150 million in peer-reviewed grants from the National Institutes of Health (NIH).
Einstein is part of Montefiore Medicine Academic Health System, an integrated academic delivery system comprising seven campuses, including 8 hospitals, a multi-county ambulatory network, a new state-of-the art “hospital without beds”, a skilled nursing facility, school of nursing, home health agency, and the state’s first freestanding emergency department. As the University Hospital for the Albert Einstein College of Medicine, Montefiore is a premier academic health system, employing Einstein’s clinical faculty and training Einstein’s medical students, over 1,300 residents, 420 allied health students, and 1,600 nursing students annually.
The Albert Einstein College of Medicine is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, age, protected veteran or disabled status, or genetic information. Einstein seeks candidates whose skills, and personal and professional experience, have prepared them to contribute to our commitment to diversity and excellence, and the communities we serve.
Tobacco use is the leading preventable cause of disease and death in the US. Over 80% of patients in substance abuse treatment, including methadone maintenance, smoke cigarettes, compared to 14% of NYC adults. Despite these high smoking rates, we know little about how to best treat tobacco use among methadone treatment patients. For this five year, NIH-funded project, we are conducting a randomized controlled clinical trial of two smoking cessation interventions: long-term medication treatment, and directly observed therapy. Research visits will include computerized research interviews, blood and urine collection, and adherence counts. The project will occur in three clinical sites in the Bronx and will follow 450 participants over a 12-month period. The Study Coordinator may also be involved in additional pilot projects.
Manage the day-to-day operations of the research project with investigators, data managers, study coordinators and clinical staff
Hire, train and supervise the study coordinator and volunteer staff
Work with the Principal Investigator (PI) to update study protocols, protocol amendments, research study measures, and study databases as needed
Create regular reports for the IRB, sponsors, and the safety monitoring board
Coordinate meetings with study partners, and represent the study at site meetings
Work with PI to develop recruitment strategies and manage tracking database; prepare regular reports for the PI about recruitment and tracking
Securely manage and maintain study data
Oversee adherence to research protocols, including conducting the study informed consent process, maintaining participant confidentiality, and collecting data
Manage and analyze data; perform regular audits to ensure that collected data are complete and accurate, and that research protocols are being followed
Conduct medical chart reviews
Supervise, coordinate and conduct research visits, data and specimen collection, data entry and data management
Lead weekly study meetings
Assist in drafting reports, preparing conference abstracts, and presentations related to the project; assist with preparation of grant proposals
Oversee budget including purchasing and payment to subjects, and generate annual financial reports
Travel to multiple clinical and research sites in the Bronx to conduct and oversee study-related activities
Troubleshoot study-related problems
Other related duties as assigned
Experience and Educational Background:
Bachelor’s in Public Health or related field. Master's Degree or minimum of 5 years experience required.
At least two years’ experience collecting data for research (e.g., recruiting participants, conducting interviews, collecting biologic specimens).
Experience working with similar populations preferred.
Skills and Competency
As part of a team, must be able to manage multiple tasks and priorities, work independently with minimal supervision, and adhere to study protocol.
Advanced working knowledge of Microsoft Word, ACCESS, Excel, and SAS or STATA.
Fluency in English and Spanish preferred.
Excellent interpersonal, organizational, and communication skills required.
Must be detail oriented.
Able to write scientific documents
Scope of Responsibility
Research Coordinator will work with Dr. Shadi Nahvi, study PI
Research Coordinator will supervise study coordinator and volunteer staff
Research Coordinator will interact regularly with clinic staff
Coordinate study-related activities between investigators, data managers, consultants, and multiple research sites