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Clinical Research Coordinator- See Description-Dept. of Medicine Dept. of Surgery

New York City, NY, United States

Posted on
Apr 07, 2021

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Company OverviewnAt Memorial Sloan Kettering (MSK), weu2019re not only changing the way we treat cancer, but also the way the world thinks about it. By working together and pushing forward with innovation and discovery, weu2019re driving excellence and improving outcomes.  Weu2019re treating cancer, one patient at a time. Join us and make a difference every day.nJob DescriptionnAre you seeking an opportunity to be at the forefront of innovation during this exciting time at **MEMBERS ONLY**SIGN UP NOW***.? This is a great role for someone who has the right skills, who wants to be part of a dynamic team and who wants to learn how to apply their skills to support our mission: the progressive control and cure of cancer through programs of patient care, research, and education.****have an exciting opportunities in a variety of Service Areas  as a Clinical Research Coordinator.  As an integral member of the research team, and in compliance with all regulatory, institutional, and departmental requirements, the Clinical Research Coordinator is responsible for the managing the clinical data. RIght now we have positions n nYou Are:nn A good decision-maker, with proven success at making timely decisions that keep the organization moving forwardn Able to hold yourself and others accountable in order to achieve goals and live up to commitmentsn An effective communicator, capable of determining how best to reach different audiences and executing communications based on that understandingn Resilient in recovering from setbacks and skilled at finding detours around obstaclesn Passionate about medical terminology and sciencen You are familiar with and excited about working with and organizing large amounts of datannYou Will:nn Collect, abstract, and enter data for research projects, databases and/or protocols (clinical trial) including reviewing patient charts, existing databases, and other sources within a specified timeframen Ensure data quality and integrity throughout the life of the study.n Collaborate with team members and individuals across MSK regarding data inputn Generate data reports and deliver to all necessary parties on the progress of research project, database or protocoln Ensure that we are following all appropriate Institutional, State, and Federal regulations throughout the study, and complete all regulatory documentation to ensure that research protocols are approved by Institutional Review Boardn Provide clerical and administrative support, such as filing and scheduling meetings and appointments as needednnYou Have:nn A Bacheloru2019s degree OR a high school diploma and 2 years of research experiencen The ability to commit to at least 2 yearsnnClosingnMSK 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, sexual orientation, national origin, age, religion, creed, disability, veteran status or any other factor which cannot lawfully be used as a basis for an employment decision.n nFederal law requires employers to provide reasonable accommodation to qualified individuals with disabilities. Please tell us if you require a reasonable accommodation to apply for a job or to perform your job. Examples of reasonable accommodation include making a change to the application process or work procedures, providing documents in an alternate format, using a sign language interpreter, or using specialized equipment.

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