Memorial Sloan-Kettering Cancer Center Clinical Research Coordinator in New York, New York
At Memorial Sloan Kettering (MSK), we’re 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, we’re driving excellence and improving outcomes. We’re treating cancer, one patient at a time.Join us and make a difference every day.
Do you want to be a part of something bigger than yourself? Are you interested in the areas of Psychology, Neuroscience, Cognition, Behavioral Health, or Science?
At MSK, we’re running one of the largest clinical trials programs for cancer in the country, and at any time we are conducting hundreds of clinical trials to improve cancer care. Spend some time with us and explore how you can find your life's calling as a Clinical Research Coordinator at MSK.
We are seeking a FULL-TIME (37.5 hours a week) Clinical Research Coordinator to assist with research protocols focused on cognition in cancer patients, and the effects of cancer care. The CRC will be responsible for recruitment of participants, data collection, and tracking participant progress throughout the studies. Additionally, the candidate will be responsible for database maintenance, data entry, communicating progress and challenges, and working with the research study team and principal investigators (PI) to manage and analyze the study data. Lastly, the prospective applicant will assist with all regulatory requirements as per MSKCC policy and federal regulations. The candidate must have superior communication skills, both written and verbal.
Recruit, consent, perform screening interviews, administer assessment batteries and collect relevant data from human subjects;
Maintain study databases, codebooks, and procedures for data entry and monitoring;
Generate reports on the progress of research projects;
Conduct regular audits, and QA of the data to ensure data accuracy and integrity;
Compile and analyze data for presentations and publications and assist with statistical analysis as needed;
Ensure that patient registration, informed consent procedures, and handling of data meet all institutional and governmental requirements;
Provide regular reports to the PI regarding study progress and challenges and work with the PI to address any problems that arise;
Complete regulatory and administrative submissions at MSKCC;
Organize and participate in weekly study meetings;
Assist in the preparation of presentations and manuscripts;
Perform literature searches and other tasks as needed
Excellent attention to detail and communication skills
Bachelor’s degree required or a high school diploma with 2 years of research experience
Excellent knowledge of Microsoft Office, databases, and SPSS helpful
Prior experience with administering neuropsychological measures and/or EEG is a plus, though not required
MSK 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.
Federal 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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Job LocationsUSA-NY-New York
Posted Date2 months ago(2/25/2021 4:18 PM)
CategoryResearch - Clinical