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Associate Research Coordinator - Brooklyn

Company: NYU Langone Health
Location: Brooklyn
Posted on: January 16, 2022

Job Description:

NYU Langone Hospital - Brooklyn is a full-service teaching hospital and Level I trauma center located in Sunset Park, Brooklyn. The hospital is central to a comprehensive network of affiliated ambulatory and outpatient practices, and serves as NYU Langone Health's anchor for healthcare access, growth, and delivery in the entire borough. Learn more about NYU Langone Hospital - Brooklyn, and interact with us on LinkedIn, Glassdoor, Indeed, Facebook, Twitter, YouTube and Instagram.Position Summary:
We have an exciting opportunity to join our team as a Associate Research Coordinator.

In this role, the successful candidate Responsible for providing basic to moderate range of coordination for Research studies conducted at the Medical Center.
Assists with recruitment, enrollment, grant submissions, research data collection and study coordination. Performs intraoperative
monitoring and serves as liaison with the IRB and the internal and external funding agencies. Ensures accurate
execution of research protocols in accordance with Good Clinical Practices, HIPAA and required obligations to
patient/subject, Principal Investigator, research team and sponsor. Interfaces directly with patients/subjects and Principal
Investigators in support of the clinical trials if applicable. Works under general supervision.Job Responsibilities:

  • Human Subjects' Research - As applicable, updates and submits necessary documents required by the NYUInstitutional Board (IRB), NYU Office of Clinical Trials and any other appropriate parties in order to obtain approvalto conduct human subjects' research. Secures accurate signatures and forwards documents and/or forms toappropriate destination. Might prepare and submit monthly enrollment statistics to the Office of Clinical Trials andprovide other information in timely manner, as necessary.Assists in the implementation and evaluation of quality improvement and assurance activities in the department,primarily in the Pre Surgical Testing area.Participates in special projects and performs other duties as required.Budgets - May develop draft budgets and submit to the Principal Investigator. Assists in the preparation of fundingreports to agencies. Helps to identify new potential sponsors/agents for trials and researches as assigned.Grants - Assists in the preparation of grant applications and related activities such as developing grants proposalsand fund raising activities. Collects and organizes required paperwork for submission if required. Follows up andcoordinates resolution of all issues progress reports to the sponsors to fund medical research in the division.Reporting and Analysis - Gathers and compiles data and assists in consolidating/analyzing data for presentation tosponsoring and regulatory agencies. Provides reports to all necessary parties (e.g., the principal investigator,sponsoring agency, etc.) on the progress of the study as needed. Conduct primary analysis to data collected.Formulates, prepares database and generates preliminary measurement reports for review by the PIContinuous Learning: Position requires ongoing continuing education in all areas of research development. It isexpected that the employee demonstrates proof of ongoing research education on a yearly basis. Trainingprograms are provided through the SOM.Clinical Competency: Position may require competency in performing EKG, phlebotomy technique, centrifuge,handling, storing and shipping of specimens. Clinical training and didactic competency tests may be required toperform basic procedures as part of position expectations. In house training and certification will be provided.Other trainings and competencies may be included as required.Recruitment - Screens potential patients/subjects for eligibility to the study and schedules the initial visits. Thismay include researching and gathering information from the medical record, physician referral, advertisement anddirectly scheduling a visit to evaluate the patient/subject. Reviews all the elements of the screening process withthe Principal Investigator that include but not limited to: inclusion/exclusion criteria, completed informed consent,documentation of the event and the patient/subject willingness to participate in the study.Research Activities - Collects patient information for the research project(s). This may include abstraction of datafrom the patient chart (e.g., laboratory or diagnostic test results, surgical/radiation treatments delivered, adversedrug reactions, etc); abstraction of data for publications, or data collection from outside physicians' offices. Usestools to facilitate data collection (e.g. calendars, schedules, tracking logs, etc). Audits and updates the database orthe case report forms. Conducts study visits, obtains and documents information within the time frame specified.Research, collects, compiles and conducts preliminary analyses of data, statistics, and other materials for reports.Conduct preliminary analysis.Study Regulations - Aware of study regulatory status and keeps an up to date copy of regulatory documents.Assists with the informed consent process and ensure that the patient/subject fully understands what is required ofthem throughout the study. Follows through regularly with the patient/subjects and reminds them of visits andcompliance.Minimum Qualifications:
    • To qualify you must have a Bachelor's degree in life sciences, allied health or equivalent in a related discipline and 0-1 years experience or an equivalent combination of education and experience.
    • Effective oral, written, communication, interpersonal skills.
    • Must be able to work under the direction of supervision.
    • Ability to operate research related equipment.
    • Proficiency in using various Microsoft Office applications such as World, Excel, Access, Power Point and Outlook. Familiar with Internet applications.
    • Ability to identify, analyze and solve problems. Time management skills and ability to work well under pressure.Preferred Qualifications:
      • Knowledge of basic medical terminology is preferred. Prior experience working with research protocols. Prior experience working in an academic medical center environment.Qualified candidates must be able to effectively communicate with all levels of the organization.

        NYU Langone Hospital - Brooklyn provides its staff with far more than just a place to work. Rather, we are an institution you can be proud of, an institution where you'll feel good about devoting your time and your talents.

        NYU Langone Hospital-Brooklyn is an equal opportunity and affirmative action employer committed to diversity and inclusion in all aspects of recruiting and employment. All qualified individuals are encouraged to apply and will receive consideration without regard to race, color, gender, gender identity or expression, sex, sexual orientation, transgender status, gender dysphoria, national origin, age, religion, disability, military and veteran status, marital or parental status, citizenship status, genetic information or any other factor which cannot lawfully be used as a basis for an employment decision. We require applications to be completed online.
        If you wish to view NYU Langone Hospital- Brooklyn's EEO policies, please click here. Please click here to view the Federal "EEO is the law" poster or visit https://www.dol.gov/ofccp/regs/compliance/posters/ofccpost.htm for more information. To view the Pay Transparency Notice, please click here.

Keywords: NYU Langone Health, New York , Associate Research Coordinator - Brooklyn, Other , Brooklyn, New York

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